WO2021250464A1

WO2021250464A1 - Non-thrombogenic devices for treating edema

Info

Publication number: WO2021250464A1
Application number: PCT/IB2021/000391
Authority: WO
Inventors: Gerry Mccaffrey; Ronan Keating; Ann Marie Cannon; Sagi Raz; Or INBAR; Eamon Brady
Original assignee: White Swell Medical Ltd
Priority date: 2020-06-08
Filing date: 2021-06-08
Publication date: 2021-12-16

Abstract

The invention provides intravascular devices for treating certain medical conditions such as edema without causing thrombosis. The intravascular devices of the disclosure include non- thrombogenic surfaces that improve blood compatibility by reducing device-related thrombus formation and inflammatory reactions. The non-thrombogenic surfaces may include surface topographies (e.g., surface roughness) and modified chemistries (e.g., coatings and/or treatments), which prevent thrombosis by reducing local shear forces and inhibiting adhesion of blood clotting factors.

Description

NON-THROMBOGENIC DEVICES FOR TREATING EDEMA

Cross-Reference to Related Applications

This application claims the benefit of and priority to U.S. Provisional Application No. 63/036,136, which was filed on June 8, 2020, and to U.S. Provisional Application No. 63/036,145, which was filed on June 8, 2020, and to U.S. Provisional Application No. 63/036,153, which was filed on June 8, 2020, and to U.S. Provisional Application No. 63/036,263, which was filed on June 8, 2020, the contents of which are each incorporated by reference.

Technical Field

This disclosure relates to devices for treating edema.

Background

Congestive heart failure occurs when the heart is too weak to pump blood properly. As a result, blood pressure increases in the veins. The increased blood pressure prevents the lymphatic system from draining fluid from surrounding tissue leading to an abnormal buildup of fluid. The abnormal buildup of fluid manifests as swollen or puffy skin and is known as edema. If untreated, edema may lead to difficulty breathing (dyspnea) and in some cases acute decompensated heart failure (ADHF).

Some attempts to treat edema have involved the use of catheters that are placed in a blood vessel and used to drain lymphatic fluid from the tissues. Unfortunately, like many devices placed in the bloodstream, intravascular catheters are susceptible to problems. Blood forms clots on the surfaces of devices placed into the bloodstream. As a clot builds up, it blocks, or occludes, the catheter and even the entire vessel itself. Such occlusions may stop the flow of blood and cause catheter malfunctions. Due to that blood clotting, also known as thrombosis, the use of intravascular catheters faces significant complications.

Summary

This disclosure provides intravascular devices, e.g., indwelling catheters, that may reside in the vasculature or other bodily lumens of patients without causing blood clots. To prevent blood clots, the disclosure provides surface treatments, materials, modifications, and chemistries that inhibit the formation of blood clots and are thus non-thrombogenic. In particular, intravascular devices of the disclosure have non-thrombogenic surfaces that inhibit activation of blood defense mechanisms and adherence of blood clotting factors. The non-thrombogenic surfaces may include specific surface topographies (e g., surface roughness) or modified surface chemistries (e.g. coatings or treatments) that improve biocompatibility of the intravascular device. Moreover, intravascular devices of the disclosure may include certain shapes that promote fluid flow patterns through the device with minimal disturbances thereby reducing shear forces otherwise associated with thrombosis.

The disclosure relates to the insight that surface roughness can contribute to thrombogenicity in medical devices as blood proteins are more apt to adhere to rougher surfaces than smoother ones. Moreover, shear forces that are associated with blood clot formation are greater in devices with rougher surfaces. As such, the invention provides intravascular devices that have optimized surface topographies to inhibit blood protein adhesion and minimize local shear forces to reduce incidences of thrombosis.

In one aspect, the invention provides an intravascular device comprising a catheter dimensioned for insertion into a vein or an artery. The catheter comprises a proximal portion and a distal portion. The catheter includes a cage attached to the distal portion. The cage houses an impeller. At least a portion of a surface of the cage or the impeller comprises a non- thrombogenic surface texture with an arithmetic average roughness (Ra) of less than 50 nanometers. The non-thrombogenic surface texture inhibits adhesion of blood proteins and reduces shear forces acting on blood on account of its smooth surface finish, thereby preventing thrombosis.

Indwelling catheters of the invention may be particularly well suited for treating edema. Clinicians may insert an indwelling catheter into a patient's jugular vein near an outlet of the patient's lymphatic duct. An impeller may be operated so as to promote an increase of blood flow through the jugular vein which, by Bernoulli’s principle, may decrease pressure at the output of the lymphatic duct and causes lymph to drain from the lymphatic system and into the circulatory system, thereby providing relief from adverse effects and symptoms of edema. Because the indwelling catheter of the invention comprises a non-thrombogenic surface, the catheter may be operated inside the patient's vein for an extended period of time to treat edema without forming blood clots.

The invention provides an indwelling catheter comprising a cage housing an impeller at a distal end, wherein at least a portion of a surface of the cage or the impeller comprises a non- thrombogenic surface texture with a Ra value of less than 50 nanometers. In some embodiments, the cage has the non-thrombogenic surface texture with a Ra value of less than 50 nanometers. In other embodiments, both the cage and the impeller have the non-thrombogenic surface texture with a Ra value of less than 50 nanometers. Preferably, substantially all exposed surfaces of the cage and/or the impeller have the non-thrombogenic surface texture, such that, while the catheter is operating inside the vein, substantially all surfaces of the cage and the impeller that contact blood will comprise the non-thrombogenic surface to maximize inhibition of blood protein adhesion.

The non-thrombogenic surface texture may be generated by processing a metal comprising one of the cage or the impeller. For example, processing may include one of tumbling, polishing, electropolishing, grinding, lapping, abrasive blasting, or similar methods used to generate a smooth surface finish. One or more of these processes may be employed during the manufacturing of the cage and/or the impeller to create and or enhance non- thrombogenic properties of the catheter. The metal comprising the cage and or the impeller may be processed until the surface roughness of the metal reaches a Ra of less than 50 nanometers. In some embodiments, the Ra value may be less than 25 nanometers.

In certain aspects, the disclosure provides a device for treating edema. The device includes a catheter having a proximal portion and a distal portion, a cage (i.e., impeller housing) attached to the distal portion of the catheter with an impeller disposed therein. At least one of the cage or the impeller comprises a non-thrombogenic surface characterized by a Ra of less than 50 nanometers, for example, 25 nanometers, or less. In preferred embodiments, the device further comprises an expandable member (e.g., a balloon) aligned over an outside of the impeller housing. An exterior surface of the expandable member may be physically coupled to an exterior surface of the impeller housing. Upon expansion of the expandable member, the expandable member may occlude the vein and direct blood flow into one or more inlets of the cage. Moreover, in an expanded configuration, the expandable member may be aligned over one or more outlets of the cage so as to mitigate blood recirculation thereby reducing shear forces that may trigger thrombosis.

In some embodiments, at least one of a portion of a cage or a portion of an impeller comprises a non-thrombogenic surface texture comprising an average depth of roughness (Rz) of less than 175 nanometers. For example, the Rz value may be about 100 nanometers. In some embodiments, the non-thrombogenic surface texture is generated by one of tumbling, polishing, electropolishing, grinding, lapping, or abrasive blasting. In other embodiments, the surface has been rendered non-thrombogenic by a treatment to reduce roughness and thereby prevent blood clotting. Reducing surface roughness may reduce local shear forces acting on blood cells passing through the catheter while the catheter is operating inside the vein.

In some embodiments, the indwelling catheter further comprises a cuff attached to a proximal portion of the cage. The cuff may provide a smooth transition between an outer surface of the catheter and a proximal portion of the cage to more easily navigate the catheter within a patient's vasculature. In some embodiments, the cuff comprises a non-thrombogenic surface texture having a Ra value of less than 50 nanometers.

In some embodiments, a distal portion of a shaft of an impeller and a proximal portion of a tip of the catheter or a proximal portion of a bearing housing define a distal gap and the distal gap comprises the non-thrombogenic surface texture. In other embodiments, a portion of the cage and a portion of the impeller define a proximal gap and the proximal gap comprises the non-thrombogenic surface texture.

Aspects of the invention provide a method for treating edema. The method includes the steps of inserting an indwelling catheter inside a patient's vein wherein the catheter includes a non-thrombogenic surface texture, the non-thrombogenic surface texture comprising a Ra value of less than 50 nanometers. Preferably, a portion of a cage or a portion of an impeller of the catheter comprises the non-thrombogenic surface texture. Preferably, both the cage and the impeller comprise the non-thrombogenic surface texture. The method further includes operating a pump (e.g., an impeller) inside the patient's vein to increase a flow of blood through the vein and create a decrease in pressure near an outlet of a lymphatic duct causing fluid to drain from the lymph and into blood circulation. The method includes modulating a flow of blood through the vein while inhibiting thrombosis on account of the catheter comprising a non-thrombogenic surface texture. In some embodiments, the catheter further comprises a pressure sensor, the pressure sensor may be designed to detect changes in blood pressure within the vein and adjust a rotational velocity of the impeller or a size of an expandable member attached to a surface of the cage accordingly. The device may include a computer system in communication with the pressure sensor.

In another aspect, the disclosure provides an intravascular device. The device comprises a catheter dimensioned for insertion into a vein or an artery. The catheter includes a proximal portion and a distal portion with a cage attached to the distal portion of the catheter. The cage houses an impeller. The cage and/or impeller surface may be configured for contact with human blood. At least a portion of a surface of the cage or the impeller comprises a non-thrombogenic surface texture with an arithmetic average roughness (Ra) that is less than a linear dimension of at least one human blood plasma protein. The human blood plasma protein may comprise albumen, fibrinogen, von Willebrand factor, or a g-globulin. Preferably, the Ra is less than 50 nanometers.

In one aspect, the invention provides an intravascular device comprising a catheter that is dimensioned for insertion into a vein. The catheter comprises a proximal portion and a distal portion with a cage attached to the distal portion. The cage housing an impeller. At least a portion of the cage or the impeller comprises a modified surface chemistry (e.g., a coating or a treatment) that minimizes or prevents formation of blood clots. In preferred embodiments, both the cage and the impeller comprise the modified surface chemistry. And preferably, substantially all of the cage and/or the impeller that is exposed to blood when the catheter is operating inside the vein comprises the modified surface chemistry.

The modified surface chemistry may provide a hydrophilic surface. The hydrophilic surface may prevent blood clots by allowing blood water to outcompete blood proteins, e.g., circulating blood clotting factors, for adhesion with the hydrophilic surface. As such, surfaces of the invention may prevent thrombosis on account of providing one or more hydrophilic surfaces that preferentially adhere with water molecules and thereby reduce plasma protein adherence on the hydrophilic surface. In some embodiments, when the catheter is inserted into the vein, the hydrophilic surface creates a layer of water molecules on the hydrophilic surface, thereby creating a barrier to plasma protein adherence by, for example, reducing or eliminating the number of binding sites for blood platelet adhesion to the hydrophilic surface. In some embodiments, the modified surface chemistry comprises a coating. The coating may be applied to the cage or the impeller; preferably both. The coating may comprise one or more of a polysaccharide, a polymer, or a hydrogel. For example, the coating may comprise the polysaccharide heparin. Heparin may provide the surface with an affinity for antithrombin. The presences of antithrombin on surfaces of the catheter may prevent blood clots by inactivating enzymes associated with the blood coagulation system.

In certain embodiments, the coating may comprise a thickness and the coating thickness may be greater than a surface texture (e.g., roughness) of the catheter. In some embodiments, the modified surface chemistry follows the contours and the roughness of the cage or the impeller. Where the modified surface chemistry creates a barrier of water when the catheter is inserted inside a vein, the layer of water may comprise a thickness that is greater than an average (Ra) of a surface of the cage or the impeller. The coating may comprise one of a polyurethane, polyethylene glycol, poly-2-oxazolines, polyvinyl alcohol, polyvinylpyrrolidone, maleic anhydride copolymer, poly(lactide-co-glycolide), aminoalkyl (meth)acrylamide, aminopropylmethacrylamide, poly-phosphorylcholine, polyethylene oxide, polyethylene succinate, polyethylene adipate, polyvinyl alcohol-co-ethylene, polyacrylic acid, copolymers and blends thereof. The coating may further comprise one of polyethyleneimine, a sulfonate group, albumin, a polyamine, polyvinyl siloxane, hyaluronic acid, or any combination thereof.

In preferred embodiments, at least one of the cage or the impeller comprises a metal having the modified surface chemistry. The metal may comprise one of scandium, titanium, vanadium, chromium, manganese, iron, cobalt, nickel, copper, or zinc. The modified surface chemistry may include a modification to an oxide layer of cage or the impeller. Modifications to the oxide layer may provide or enhance hydrophilic properties of a surface of the catheter. Hydrophilic properties may allow surface to bind to water molecules to the exclusion of plasma proteins. Modifying the oxide layer may increase surface wettability. The surface wettability may have a contact angle measurement of less than 20 degrees. The oxide layer may be modified by one of heat treatment, electropolishing, or acid passivation. Modification of the oxide layer may result in an oxide layer having a thickness that is less than 5000 picometers, less than 3000 picometers, or less than 2000 picometers. Modification of the oxide layer may result in an oxide layer thickness greater than 200 picometers, greater than 400 picometers, or greater than 600 picometers. The cage and/or the impeller may comprises a transition metal from period 4, D- block of the periodic table and the oxide comprises an oxide of said period 4 transition metals.

In some embodiments, the cage and/or impeller comprise a surface layer and the surface layer comprises an enriched concentration of titanium or chromium. The surface layer may comprise a metal oxide of titanium oxide (TiO), titanium dioxide (Ti02), dititanium trioxide (Ti203), chromium (II) oxide (CrO), chromium (III) oxide (Cr203), chromium dioxide (Cr02), chromium trioxide (Cr03), chromium (IV) or any combination thereof.

In certain embodiments, the hydrophilic surface may be characterized as comprising a water contact angle of 20 degrees or less, for example, the hydrophilic surface may comprise a water contact angle of 10 degrees or less. In certain embodiments, the modified surface chemistry comprises a super-hydrophilic surface, for example, with a water contact angle of less than 10 degrees.

In some embodiments, the modified surface chemistry comprises a hydrophilic functional group. The hydrophilic functional group may comprise one or more of a hydroxy group, a carboxyl group, an amine group, a carbonyl group, a chloro group, an ether group, or a phosphate group.

In some embodiments, the modified surface chemistry comprises a first atom and a second atom, the first atom forming a chemical bond with an oxide layer of a surface of the cage and/or impeller and said second atom forming a bond with said first atom. The first atom comprising a first electronegativity and the second atom comprising a second electronegativity and the difference between said electronegativities is equal to or greater than 0.8, or is equal to or greater 1.0, or is equal to or greater 1.2, or is equal to or greater 1.5.

In some embodiments, the catheter further comprises a cuff. The cuff may provide a smooth transition between an outer surface of the catheter and a proximal portion of the cage.

The cuff may comprise a modified surface chemistry, such as a coating or a treatment. In some embodiments, a distal portion of a shaft of the impeller and a distal portion of the cage defines a gap. At least one of the distal portion of the shaft or the distal portion of the cage defining the gap comprises the modified surface chemistry so as to prevent blood from clotting the gap.

In some aspects, devices of the invention are useful for treating edema. Devices may include a catheter that is dimensioned for insertion into a vein, such as a jugular vein. The catheter comprises a proximal portion and a distal portion with a cage attached to the distal portion. The cage housing an impeller. An expandable member may be attached to an exterior surface of the cage. The expandable member may be, for example, a balloon. Expansion of the expandable member may stabilize the distal portion of the catheter inside the vein and also help to impede and direct fluid flow into one or more inlets disposed on the cage. The expandable member may be shaped so as to direct fluid flow into the inlets without creating disturbances in the flow, thereby reducing shear forces acting on blood particles to further reduce incidences of thrombosis.

Aspects of the invention provide a method for treating edema. The method includes the steps of inserting an indwelling catheter inside a patient's vein wherein the catheter includes a modified surface chemistry comprising one of a treatment or a coating. Preferably, a portion of a cage or a portion of an impeller of the catheter comprises the modified surface chemistry. Preferably, both the cage and the impeller comprise the modified surface chemistry. The method further includes operating an impeller inside the patient's vein to increase a flow of blood through the vein and create a decrease in pressure near an outlet of a lymphatic duct causing fluid to drain from the lymph and into blood circulation. The method includes modulating a flow of blood through the vein while inhibiting blood clot formation on surfaces of the catheter on account of the catheter comprising the modified surface chemistry. Preferably, the modified surface chemistry enhances hydrophilic properties of the surface of the catheter. In some embodiments, the modified surface chemistry comprises a coating. The coating may comprise heparin. In other embodiments, the modified surface chemistry comprises a treatment that modifies a surface oxide layer. Modification of the oxide layer may provide the catheter with a super-hydrophilic surface. In some embodiments, the catheter further comprises a pressure sensor, the pressure sensor may be designed to detect changes in blood pressure within the vein and adjust a rotational velocity of the impeller or a size of an expandable member attached to a surface of the cage accordingly. The device may include a computer system in communication with the pressure sensor.

In one aspect, the disclosure provides a device for treating edema. The device includes a catheter dimensioned for insertion into a vein such as a jugular vein. The catheter comprises a proximal portion and a distal portion with a cage attached to the distal portion. The catheter further includes an expandable member attached to an exterior surface of the cage. A portion of a surface of the expandable member is non-thrombogenic. The surface may be non-thrombogenic on account of a hydrophilic material or coating. Preferably, the expandable member surrounds the cage and comprises a shape (e.g., a toroid shape) that facilitates blood flow into one or more inlets of the cage without creating disturbances in blood flow.

In some embodiments, the non-thrombogenic surface comprises a hydrophilic coating or a hydrophilic material. The non-thrombogenic coating or material may prevent thrombosis by associating with water molecules to the exclusion of blood plasma proteins (e.g., blood clotting factors), thereby preventing the formation of blood clots on the surface. Preferably, the non- thrombogenic surface comprises a coating. In some embodiments, the surface of the expandable member includes portions with the hydrophilic coating and portions without the hydrophilic coating. The one or more portions with and without the hydrophilic coating may form a pattern. The pattern may be more apparent when the expandable member is in an expanded state. The pattern may increase non-thrombogenic properties of the surface and further help to reduce blood clotting. For example, the pattern may disrupt blood proteins from binding to surfaces of the catheter. The pattern may comprise one of stripes, spirals, waves, or may be a zebra pattern.

The non-thrombogenic surface may comprise a hydrophilic coating. The coating may include one of a polysaccharide, a polymer, and a hydrogel. For example, the non-thrombogenic surface may include a polymer comprising silicon. In other embodiments, the non-thrombogenic surface may include a polysaccharide. The polysaccharide may be heparin. Preferably, the hydrophilic coating comprises more than half of the surface of the expandable member that is exposed to blood when the expandable member is in an expanded state inside the vein. In other embodiments, the non-thrombogenic surface comprises a hydrophilic material. The hydrophilic material may comprise one of polyethylene terephthalate, polyamide, polyurethane, or nylon; preferably, polyurethane.

In preferred embodiments, the expandable member comprises a balloon. Upon expansion of the balloon, the balloon opposes a wall of a blood vessel and helps direct blood flow into one or more inlets on the cage. The balloon my comprise a toroid shape. The shape of the expandable member (e.g., balloon) may help to prevent thrombosis by minimizing disturbances in fluid flow, thereby inhibiting shear forces acting on blood particles. The cage may further comprise one or more outlets through which fluid exits. In preferred configurations, a distal-most portion of the expandable member (e.g., balloon), is aligned over the outlets to mitigate blood recirculation when the catheter is operating inside the blood vessel. In some embodiments, the non-thrombogenic surface comprises a block copolymer. The block copolymer comprising a first polymeric block and a second polymeric block. The first polymeric block may include a hydrophilic functional group. The second polymeric block may include a polymer repeat unit. The polymer repeat unit may be selected to enhance flexibility in the second polymeric block. The first and said second polymeric blocks may be substantially immiscible and, when copolymerized, may form phase separated blocks within a polymer matrix. The phase separation may be manifested or apparent on the surface of said expandable member. In some embodiments, the polymer comprises non-bound chemical species, the non bound chemical species comprising oligomers and additives. The polymer may be treated so as to remove non-bound chemicals and further manifest the phase separation on the surface of the expandable member. Removal of the non-bound chemicals may improve hydrophilicity.

In certain embodiments, the catheter includes an expandable member with a non- thrombogenic surface. The non-thrombogenic surface may comprise a hydrophilic coating that attracts water molecules to prevent blood clotting factors from binding. The surface of the expandable member may include portions with the hydrophilic coating and portions without the hydrophilic coating. The portions with the hydrophilic coating may be configured for continuous contact with blood when the expandable member is in an expanded state. The portions without the hydrophilic coating may be configured to maintain a static contact with the vessel wall when the expandable member is in an expanded state. The expandable member may be configured to maintain static contact with the wall of the vein in the expanded state when the pressure gradient across the expandable member is between lmmHg and 30mmHg.

In some embodiments, the expandable member comprises a hydrophilic coating and the hydrophilic coating comprises one selected from the group consisting of a polysaccharide, a polymer, and a hydrogel. The polymer may comprise a polymer with a hydrophilic chain segment. The polymer may comprise a block copolymer with a hydrophilic block and a hydrophobic block, wherein the hydrophobic block is configured to bind to the surface of an expandable membrane of the expandable member. In embodiments in which the expandable member comprises a polysaccharide, the polysaccharide may comprise a polymeric derivative of heparin. In some embodiments, the hydrophilic material comprises one of an aromatic polyurethane, an aliphatic polyurethane, a polyurethane comprising a copolymer of polytetramethylene glycol, a polyurethane comprising a copolymer of polyethylene glycol, a polyurethane comprising a copolymer of polypropylene glycol, a polyurethane comprising a copolymer of a polycarbonate glycol or a blend, copolymer or mixture of the above.

In preferred embodiments, the expandable member comprises a balloon. The balloon includes at least two states: a collapsed state for delivery and retraction, and an expanded state for treatment. In the collapsed state, a membrane of the expandable member is substantially unstressed and in the expanded state the membrane is stressed by inflation pressure of the balloon. Expansion of the balloon may comprise an unfolding of a balloon membrane. The expanded state may comprise a radial expansion of a tubular segment of the balloon. Radial expansion of the tubular segment may comprise an increase in the circumference of the balloon of 300%, 400%, or 500%, or greater. For example, in some embodiments, the balloon may be designed to expand along a circumference without a corresponding expansion along a length of the balloon. Alternatively, the radial expansion of the tubular segment may comprise a biaxial elongation of a wall of the tubular segment. The radial expansion of the tubular segment may comprise a circumferential elongation and an axial elongation of a wall of the balloon with both axial and circumferential elongations occurring at the same time as the tubular segment expands. Preferably, in the expanded state, a surface of the expandable member is non-thrombogenic. The balloon, in the expanded state, may comprise a circumference or a wall thickness that is less than 50% of the circumference or wall thickness of the balloon in the collapsed state. The balloon, in the expanded state, may comprise a circumference or wall thickness that is less than 30% of the circumference or wall thickness of the balloon in the collapsed state, for example, less than 20%, or less than 15%.

The expandable member may comprise a balloon. The balloon may comprise an elastomer. The elastomer may comprise thermoplastic polyurethane, for example, such as the elastomer sold under the trade name Tecoflex or Pellethane by Lubrizol; or the elastomer sold under the trade name Texin by Covestro. The elastomer may comprise a polycarbonate urethane, for example, such as the elastomer sold under the trade name ChronoFlex by AdvanSource Biomaterials. The elastomer may comprise an aromatic polyurethane, for example, such as the elastomer sold under the trade name Polyblend by AdvanSource Biomaterials. The elastomer may comprise a thermoplastic rubber, for example, such as the elastomer sold under the trade name Chronoprene by AdvanSource Biomaterials. The elastomer may comprise aliphatic polyether-based urethanes, for example, such as the elastomer sold under the trade name Chronothane by AdvanSource Biomaterials. The elastomer may comprise a thermoplastic silicone polycarbonate, for example, such as the elastomer sold under the trade name Chronosil by AdvanSource Biomaterials. The elastomer may comprise a thermoplastic block copolymer, for example, such as the elastomer sold under the trade name Desmopan by Covestro. The elastomer may comprise thermoplastic polyurethane, for example, such as the elastomer sold under the trade name Ellastolan by BASF; or the elastomer sold under the trade name Hyperlast by Dow Engineering; or the elastomer sold under the trade name Tecophilic or Tecobax by Lubrizol. The elastomer may comprise an equivalent of the aforementioned exemplary elastomers or a blend of the aforementioned elastomers. A balloon wall material may comprise a resilient elastomer material with a low hysteresis loss ratio at human body temperature. The hysteresis loss ratio of the balloon wall material may be less than 30% at a maximum test elongation of 300% at human body temperature. The hysteresis loss ratio of the balloon wall material may be less than 20% at a maximum test elongation of 300% at human body temperature. The hysteresis loss ratio of the balloon wall material may be less than 150% at a maximum test elongation of 300% at human body temperature. The balloon wall material may comprise a low hysteresis loss ratio at human body temperature across a range of maximum test elongations and across a range of test times.

The balloon wall material may be configured to resist creep when inflated in a patient to a diameter of an innominate vein or superior vena cava vein. The material creep resistance may comprise returning the balloon to substantially its original deflated state after being inflated in a patient to a diameter of the innominate vein or the superior vena cava vein and then inflated again. The balloon wall material creep resistance may comprise the external surface area of the deflated balloon remaining substantially unchanged after an inflation and deflation cycle to a diameter of the innominate vein or the superior vena cava vein at human body temperature. The inflation and deflation cycle may comprise a plurality of inflation and deflation cycles over a time period of 24 hours. The inflation and deflation cycle may comprise a plurality of inflation and deflation cycles over a time period of 72 hours.

In some embodiments, the device of the invention includes a catheter dimensioned for insertion into a vein or an artery. The catheter includes an expandable member attached to an exterior surface of a cage. An exterior surface of the cage comprises a proximal attachment surface and a distal attachment surface with the expandable member attached to said proximal and distal attachment surfaces. The proximal and distal attachment surfaces may comprise interstitial surfaces. The interstitial surfaces may comprise a multiplicity of asperities and a plurality of interstices, wherein attachment of the expandable member to the interstitial surfaces comprises an interpenetration of some of the material of the expandable member around the asperities of the interstitial surface and into the interstices of the interstitial surfaces. The interstitial surfaces may comprise a surface roughness (Ra) that is equal to or greater than 1 micrometer, for example, greater than 3 micrometers, or greater than 9 micrometers. The proximal attachment surface and said distal attachment surface may comprise a single tubular surface with a proximal end and a distal end.

Aspects of the invention provide a method for treating edema. The method includes inserting an indwelling catheter inside a patient's vein in the vicinity of an outlet of a lymphatic duct. The catheter includes an impeller assembly attached to a distal portion. The impeller assembly comprises a cage housing an impeller with an expandable member operably associated with an outer surface of the cage. The expandable member comprises a non-thrombogenic surface that inhibits formation of blood clots during treatment of edema. The method further includes operating the impeller inside the patient's vein to increase a flow of blood through the vein. Increasing blood flow through the vein creates a decrease in pressure near the outlet of the lymphatic duct causing fluid to drain from the lymph and into blood circulation. As such, methods of the disclosure include modulating a flow of blood through the vein while inhibiting blood clot formation on surfaces of the catheter on account of expandable member comprising a non-thrombogenic surface. In some embodiments, the non-thrombogenic surface is provided by a coating. The coating may comprise heparin. In other embodiments, the non-thrombogenic surface comprises a non-thrombogenic material. For example, the expandable member may comprise polyurethane. In some embodiments, the catheter further comprises a pressure sensor, the pressure sensor may be designed to detect changes in blood pressure within the vein and adjust a rotational velocity of the impeller or a size of an expandable member attached to a surface of the cage accordingly. The device may include a computer system in communication with the pressure sensor.

In one aspect, the disclosure provides an intravascular device. The device includes a catheter dimensioned for inserting into a vein such as a jugular vein. The catheter includes a proximal portion and a distal portion with a cage attached to the distal portion. The cage houses an impeller. A portion of a surface of the cage or the impeller comprises a non-thrombogenic metallic interface. The non-thrombogenic metallic interface involves a portion of the catheter that is intended to be contact with blood while the catheter is operating inside the vein. The non- thrombogenic metallic interface can be a metal oxide film. The non-thrombogenic metallic interface can be a non-thrombogenic metal. In some embodiments, the cage has the non- thrombogenic metal. In preferred embodiments, both the cage and the impeller comprises the non-thrombogenic metal. For example, substantially all of the surface of the cage and/or the impeller that is in contact with blood when the catheter is inside the vein may have the non- thrombogenic metal.

In preferred embodiments, the non-thrombogenic metallic interface includes a transition metal or a post-transition metal. For example, the non-thrombogenic metal of the interface may include one or more of titanium, cobalt, nickel, zirconium, gold, silver, or iridium, aluminum, tin, gallium, stainless steel, tantalum, or nickel titanium. Preferably, the non-thrombogenic metallic interface exhibits hydrophilic properties that inhibit formation of blood clots while the catheter is inside the vein. The hydrophilic properties may inhibit the formation of blood clots by preferentially associating with molecules of water present in blood to the exclusion of circulating blood clotting factors. The metal may preferentially interact with water molecules at partially due to the electronegativity status of selected elements comprising the metal.

In some preferred embodiments, the non-thrombogenic interface involves a non- thrombogenic metal is treated to enhance hydrophilic properties of a surface of the metal. The treatment may make the metal super-hydrophilic. For example, the non-thrombogenic metal may include titanium, and the treatment may include a surface oxide treatment that alters or modifies an oxide layer on the surface of the metal. Modifications to the oxide layer may include changes in thickness, topography, and chemical composition. Such modifications may improve surface wettability and reduce adherence of blood clotting factors. In some instances, the oxide layer is formed or modified by one of electropolishing, heat treatment, or acid passivation. In some embodiments, the surface oxide treatment may remove and generate a new oxide layer that is substantially uniform across the surface of the metal. A substantially uniform oxide layer may provide improved hydrophilic properties.

For example, in some embodiments, the non-thrombogenic metallic interface involves a metal oxide film. The metal oxide film involving properties of an oxygen active material, which is a material that spontaneously forms an oxide when exposed to oxygen without the need for a catalyst to facilitate the reaction. The oxygen active material can be a material that spontaneously forms an oxide when exposed to air or an atmosphere with a similar oxygen content to air.

In some embodiments, the catheter further includes a cuff attached to a proximal portion of the cage. The cuff provides a smooth transition between the cage and the catheter. Preferably, the cuff includes the non-thrombogenic metal. For example, substantially all of the cuff that is in contact with blood when the catheter is inside the vein may comprise the non-thrombogenic metal.

In some embodiments, the catheter further includes an expandable member attached to an exterior surface of the cage. Preferably, the expandable member comprises a balloon. When the distal portion of the catheter is inside the vein, the expandable member may be inflated and the impeller may be activated so as to draw blood through the cage. Increasing the flow of blood through the cage may reduce pressure near a lymph duct. Reducing pressure near the lymphatic duct may cause lymph to drain into the circulatory system, thereby treating symptoms associated with edema.

Embodiments of the disclosure provide an impeller assembly shaped to minimize shear forces acting on blood particles traveling through the impeller assembly. Minimizing shear forces may help reduce incidences of thrombosis. In some embodiments, the cage is shaped to increase a flow of fluid traveling through the cage. For example, the cage may include stepped portions that define changes in inner diameters within the cage to increase the flow of fluid therein. In some embodiments, for example, a lumen of the cage may be narrower at a proximal portion than at a distal portion. In other embodiments, the lumen of the cage may taper towards, for example, the distal end. In some embodiments, the cage comprises a cross-sectional diameter of an outer wall of the cage that is greater at a proximal portion than at a distal portion.

In some embodiments, the catheter further comprises an atraumatic tip extending from a distal portion of the cage. The atraumatic tip may prevent damage to epithelial cells while navigating the catheter inside a patient’s vasculature. Preventing damage to the epithelial cells may prevent thrombosis. The atraumatic tip comprises polyether ether ketone. The atraumatic tip may include a bull nose tip. The atraumatic tip may include a metallic, which may be, for example, a distal portion of the metal cage. The atraumatic tip may include a polymer tip. The polymer tip may be an elongate flexible member. The polymer tip may be a pig tail, e.g., ending in a tightly curled tip that resembles the tail of a pig. The atraumatic tip may include an elongate member of increasing flexibility, which is useful to guide a distal end of the catheter through a vasculature system without poking or tearing a blood vessel.

Aspects of the invention provide a method for treating edema. The method includes the steps of inserting an indwelling catheter inside a patient's vein in the vicinity of an outlet of a lymphatic duct. The catheter includes an impeller assembly attached to a distal portion. The impeller assembly comprises a cage housing an impeller. At least one of the cage or the impeller has a non-thrombogenic metal. The method further includes operating the impeller inside the patient's vein to increase a flow of blood through the vein. Increasing blood flow through the vein creates a decrease in pressure near the outlet of the lymphatic duct causing fluid to drain from the lymph and into blood circulation. As such, methods of the disclosure include modulating a flow of blood through the vein while inhibiting blood clot formation on surfaces of the catheter on account of the non-thrombogenic metal. In some embodiments, the non- thrombogenic meal includes titanium with a surface oxide treatment. The oxide surface treatment may enhance hydrophilic properties of the metal. In some embodiments, the catheter further comprises a pressure sensor, the pressure sensor may be designed to detect changes in blood pressure within the vein and adjust a rotational velocity of the impeller or a size of an expandable member attached to a surface of the cage accordingly. The device may include a computer system in communication with the pressure sensor.

In other aspects, the disclosure provides an intravascular device comprising a catheter dimensioned for insertion into a vein or an artery. The catheter includes a proximal portion and a distal portion with a cage attached to the distal portion. The cage houses an impeller, and a portion of a surface of the cage or the impeller comprises a non-thrombogenic metallic interface. The non-thrombogenic metallic interface can be a non-thrombogenic metal. In some embodiments, the non-thrombogenic metal comprises a primary metallic element, wherein said primary metallic element is selected from the period 4 transition metals of the periodic table. Period 4 transition metals starts at scandium and continues to zinc and includes titanium, chromium, iron, cobalt and nickel, all of which would be a preferred metal for alloys of the invention. The non-thrombogenic metal may comprise a secondary metallic element, wherein said secondary metallic element includes one of : (i) the group of period 4 transition metals of the periodic table; or (ii) molybdenum from period 5 of the periodic table; or (iii) tungsten, gold, tantalum or platinum from period 6 of the periodic table. The non-thrombogenic metal may comprise an alloy. The non-thrombogenic metal alloy may comprise an alloy of chromium or an alloy of titanium. The non-thrombogenic metal may comprise a chromium alloy such as a stainless-steel alloy or the non-thrombogenic metal may comprise a cobalt chromium alloy. The non-thrombogenic metal may comprise a titanium alloy such as nitinol, Ti6A14V or 4TITUDE. The nitinol may comprise undesirable inclusions (small particulate impurities). Preferably the nitinol grade comprises a low level of inclusions. The non-thrombogenic metal may comprise a cobalt chromium alloy. The chromium alloy may comprise nickel, for example, such as the alloy sold under the trade name MP35N by NeoNickle; or sold under the trade name L-605; or sold under the trade name Elgiloy by Elgiloy. The alloy may be non-magnetic. In some embodiments, the metal comprises a metal grade associated with a low level of undesirable impurities, wherein said undesirable impurities comprise nitride, sulfide, silicate, phosphide, carbide, or hydride impurities. The non-thrombogenic metal may comprise a surface comprising an oxygen active material. The non-thrombogenic metal surface may comprise an oxide of said oxygen active material. The oxygen active material may comprise titanium or chromium or aluminum. The non-thrombogenic interface can be a metal oxide film. The metal oxide film may be useful to prevent scratching or corrosion of a surface of the catheter. Advantageously, by preventing scratching or corrosion, the metal oxide can reduce development of thrombosis. The metal oxide may be an amorphous oxide film. The film may comprise a thickness beneficial for preventing thrombosis. The thickness of the film may be, for example, between 5 and 50 nanometers. For example, the thickness may be about 25 nanometers.

The oxygen active material may be a material that spontaneously forms an oxide when exposed to oxygen without the need for a catalyst to facilitate the reaction. For example, the oxygen active material may be a material that spontaneously forms an oxide when exposed to air or an atmosphere with a similar oxygen content to air.

In some embodiments, the non-thrombogenic metal comprises a surface with a continuous oxide film across the surface, for example, on one of the cage or the impeller. Preferably, the cage or the impeller comprises a metallic substructure said metallic substructure enveloped with a continuous oxide film said oxide film defining an exterior surface of the cage or the impeller. The oxide film may comprise an oxide film of a metallic element of said metallic substructure. The oxide film may be configured so as to substantially preclude oxides of thrombogenic metallic elements and/or promote oxides of non-thrombogenic elements. For example, the oxide film may be configured to promote titanium dioxide or chromium oxide or the oxide film may be configured to preclude oxides of nickel, iron, cobalt, copper and zinc. In certain embodiments, the oxide film comprises Ti02 or Cr203 or A1203 or a mixture of two or more of these oxides. For example, at least 90%, 95%, or 98%, of the metal content of the oxide film may comprise Ti02 or Cr203 or A1203 or a mixture thereof. In some embodiments, the non-thrombogenic metal comprises a plurality of hydrophilic groups attached to the oxide film. In some embodiments, the attachment of a plurality of hydrophilic groups comprises a chemical attachment of said reactive groups to the oxide film. The attachment of the hydrophilic groups may comprise a chemical modification of the oxide film. The attachment of the hydrophilic groups may involve a chemical attraction, for example, an ionic attraction or covalent bond.

The non-thrombogenic metallic interface may include a hydrophilic coating. The hydrophilic coating may comprise a plurality of polymer chains. The plurality of polymer chains comprises a hydrophilic region and a substrate attachment region. The substrate attachment region may include at least one chemical functional group having functional properties for bonding with a metal surface or a metal oxide surface. The substrate attachment region may include a plurality of functional groups that in unison bond to the metal surface or metal oxide surface. The plurality of functional groups may include a polymer chain. The plurality of functional groups may include a hydrophobic polymer chain. In some embodiments, the plurality of functional groups includes a triol. The triol may include a chain end of a hydrophilic polymer chain. The triol may include a R- 1,1,1 triol. In some embodiments, the plurality of functional groups of the coating comprises a silane. The plurality of functional groups may be an acrylic. In certain embodiments, the substrate attachment region of the polymer chains includes a reactive chain end where said reactive chain end is reactive to a metal or metal oxide substrate. The thickness is preferably small in comparison to the gap region between the impeller and the cage. The coating thickness can be, for example, less than 20%, 10%, 5% or 2% of the gap region between the impeller and the cage.

Brief Description of Drawings

FIG. 1 shows an intravascular device.

FIG. 2 shows a partial cutaway view of an impeller assembly. FIG. 3 shows an inlet of an impeller assembly.

FIG. 4 shows an outlet of an impeller assembly.

FIG. 5 shows a portion of a cage comprising an inlet with a non-thrombogenic surface. FIG. 6 shows an impeller.

FIG. 7 shows an impeller assembly with an expandable member.

FIG. 8 shows a distal view of an impeller assembly.

FIG. 9 shows an impeller.

FIG. 10 shows an inlet region of a cage with a cuff removed.

FIG. 11 shows an exemplary cage.

FIG. 12 shows a scanning electron microscope image of a surface of a conventional metal cage at high magnification.

FIG. 13 shows plasma proteins and interstices of a surface with a Ra of 800 nanometers. FIG. 14 shows plasma proteins and interstices of a surface with a Ra of 50 nanometers. FIG. 15 shows a metal substrate with a modified surface chemistry.

FIG. 16 shows a portion of the periodic table with electronegativity (EN) values.

FIG. 17 shows a schematic stress strain curve for an elastomer.

FIG. 18 shows an exemplary impeller assembly with an expandable member in a collapsed state.

FIG. 19 shows an exemplary impeller assembly an expandable member.

FIG. 20 shows an alternative embodiment of an expandable member.

FIG. 21 shows an alternative expandable member balloon of the invention.

FIG. 22 shows a surface roughness characterization of a portion of a surface of a cage. FIG. 23 shows a surface roughness characterization of a portion of cage.

FIG. 24 shows a standard microscopy image of a surface of a cage.

FIG. 25 shows a portion of the periodic table of elements.

FIG. 26 illustrates a cross sectional view of a portion of a metallic body comprising a cage or an impeller.

FIG. 27 shows a schematic of a lattice structure of a surface fdm.

FIG. 28 shows a triol coupling agent. Detailed Description

This disclosure relates to devices and methods for treating medical conditions such as edema or congestive heart failure. The disclosure provides intravascular devices, e.g., indwelling catheters, capable of residing in a patient's bloodstream for prolonged periods of time without causing thrombosis. The intravascular devices of the disclosure include non-thrombogenic surfaces that improve blood compatibility by reducing device-related thrombus formation and inflammatory reactions. The non-thrombogenic surfaces provided by this disclosure include surface topographies (e.g., surface roughness) and modified chemistries (e g., coatings and/or treatments), which prevent thrombosis by reducing local shear forces and inhibiting adhesion of blood clotting factors. Moreover, intravascular devices provided by the disclosure include certain geometric features to efficiently manipulate fluid flow patterns through the device with minimal disturbances to further reduce shear forces acting on blood.

Intravascular devices of the invention are designed to inhibit and/or prevent thrombosis on account of optimized fluid flow patterns and surfaces that inhibit activation of blood defense mechanisms and adherence of certain blood clotting factors. In some aspects, the disclosure relates to non-thrombogenic materials and surface modifications for use in indwelling catheters such as those described in co-owned world application PCT/US2020/019901, which is incorporated herein by reference.

FIG. 1 shows an intravascular device 101. The device 101 comprises a catheter 103 dimensioned for insertion into a vein, such as, a jugular vein, a subclavian vein, an axillary vein, femoral vein, etc. The catheter 103 may be dimensioned for insertion into a vein on account of its size and shape. The catheter 103 has a proximal portion 107 and a distal portion 109. Preferably the distal portion 109 comprises an impeller assembly 111 comprising a cage 113 with an impeller rotatably disposed therein. In preferred embodiments, an expandable member 115 is attached to an outer surface of the cage 113. The expandable member 115 may comprise a deployed and collapsed configuration and in the deployed configuration may help anchor the device inside of the vein and also function to impede, inhibit, or direct blood flow. The collapsed configuration may be helpful for delivery and retrieval of the catheter 103.

When a distal portion 109 of the intravascular device 101 is inserted into a vein, such as a jugular vein, the device may be operated so that the impeller disposed within the cage 113 rotates. The rotation of the impeller can create a force which urges fluid (e g., blood) through the cage 113. In preferred embodiments, the intravascular device 101 may be used to treat edema. The intravascular device may, for example, be inserted into a jugular vein and directed into the vicinity of an outlet of a lymphatic duct. The impeller may be operated by, for example, turning on a motor that is operably connected to the impeller via a drive cable disposed within the catheter 103, thereby causing the impeller to rotate and urging fluid through the cage 113. According to Bernoulli's principle, the increase in flow of fluid through the jugular vein may cause a decrease in pressure near the outlet of the lymphatic duct, thereby causing fluid (e.g., lymph) to drain from lymph duct and into the blood stream.

FIG. 2 shows a partial cutaway view of an impeller assembly 211. The impeller assembly 211 includes a cage 213 housing an impeller 217. In preferred embodiments, the impeller assembly 211 includes an expandable member 215 aligned over an outer surface of the cage 213. The cage 213 may be attached to a distal portion 209 of the catheter 203. When the impeller 217 is operated inside a vein, fluid, such as blood, is pulled into one or more inlets 219 disposed on a proximal portion of the cage 213. The fluid then flows through the cage 213 and is propelled out one or more outlets 221 of a distal portion of the cage 213. Preferably, the impeller assembly 211 is shaped such that as fluid flows through the cage 213 via the inlets 219 and outlets 221, the fluid exhibits a smooth laminar flow without disturbances such as recirculation or vortices. A smooth laminar flow is advantageous as it may reduce shear forces acting on particles within the fluid, e.g., blood cells, which may otherwise cause unwanted affects, e.g., blood clots.

In some aspects, the invention provides a thrombosis-resistant intravascular device, such as an indwelling catheter 203. The catheter 203 may include an impeller assembly 211 with a cage 213 housing an impeller 217 connected to a distal portion 209 of the catheter 203. At least a portion of a surface 225 of the cage 213 and/or the impeller 217 comprises a non-thrombogenic surface texture, i.e., surface roughness.

Thrombogenicity refers to the tendency of a material in contact with the blood to produce a thrombus, or clot. It not only refers to fixed thrombi but also to emboli, thrombi which have become detached and travel through the bloodstream. Thrombogenicity may include events such as the activation of immune pathways and the complement system. In general, all materials are considered to be thrombogenic to a degree with the exception of endothelial cells which line blood vessels. As used herein, non-thrombogenic materials or surfaces refer to materials or surfaces with properties which reduce thrombogenicity. As such, the non-thrombogenic materials or surfaces described herein refer to materials and surfaces comprising features that reduce incidences of thrombosis.

Thrombus formation may be the result of at least two interdependent mechanisms, platelets and circulating protein clotting factors. Platelets, small anuclear cells that circulate in blood in ranges from 150 x 106/mL to 400 x 106/mL are one component of hemostasis. Activation of platelets by a variety of stimuli initiate complex pathways that result in platelet aggregation and the release of potent pro-thrombotic molecules. Blood contact with artificial surfaces may elicit platelet activation by a variety of mechanisms, including device related alteration in blood flow that trigger shear-related platelet activation, and due to direct platelet adherence to the deposited protein layer on synthetic surfaces of the device. Activated platelets undergo dramatic shape changes which promote aggregation with other platelets, and release platelet and pro-coagulant agonists (such as thromboxane A2, ADP, and FVa). The phospholipids of the platelet membrane also serve as the substrate for activated clotting factors, resulting in local amplification of the coagulation cascade. Aggregation of platelets, together with explosive activation of protein clotting factors, may result in significant thrombus accumulation on the device surface, embolization of thrombus particles into the bloodstream, and may cause detectable reductions in circulating platelet count (consumption of platelets).

Roughness plays an important role in determining how an object will interact with its environment, and in the context of the present disclosure, plays an important role in determining how blood will interact with the intravascular device by influencing whether blood clots are likely to form. A smooth surface is less likely to initiate a blood defense mechanism such as causing the formation of a blood clot than a rough surface.

The non-thrombogenic surface texture may be characterized by its arithmetic average roughness (Ra), which is the arithmetic average of absolute values of roughness profile ordinates. In particular, Ra is the arithmetic average of the absolute values of the measured profile height deviations taken within the sampling length and measured from the graphical center line. Surface roughness, as measured by Ra, is a component of surface texture and may be quantified by the deviations in the direction of the normal vector of a real surface from its ideal form. If the deviations are large, the surface is rough; if they are small, the surface is smooth. Preferably, the deviations are small. Ra is generally expressed in micrometers. Although, as used herein, Ra values shall are expressed in nanometers. In some aspects, the disclosure provides an indwelling device, e g., a catheter, comprising a surface texture with a Ra of less than 75 nanometers.

Surface roughness measurements, such as Ra, may be measured using atomic force microscopy (AFM), for example, as described in Webb, 2012, Roughness Parameters for Standard Description of Surface, Nanoarchitecture, Scanning: Vol. 34, 257-263, incorporated by reference. Alternatively, surface roughness may be measured using a surface roughness tester such as the surface roughness tester sold under the trade name Phase II, SGR-4600, Surface Roughness Tester/Profilometer by Phase II (Upper Saddle River, NJ).

In preferred embodiments, at least a portion of a surface of the cage 213 or the impeller 217 comprises a non-thrombogenic surface texture with a Ra value of less than 50 nanometers. Preferably, the Ra value is less than 25 nanometers. In some embodiments, at least a portion of the cage 213 comprises the non-thrombogenic surface texture. The portion of the cage 213 comprising the non-thrombogenic surface texture may be substantially all of exposed portions of the cage 213 that contacts blood when the device is operating inside a vein. In other embodiments, only portions of the cage 213 that comprise the inlets 219 and/or outlets 221 may have the non-thrombogenic surface texture as these areas may be more prone to blood protein adhesion or blood particle shearing due to certain patterns of fluid flow. In some embodiments, at least a portion of the impeller 217 comprises the non-thrombogenic surface texture with a Ra value of less than 50 nanometers. For example, the portion of the impeller 217 that contacts blood while the impeller 217 is operating inside the vein may comprise the non-thrombogenic surface texture to prevent blood proteins from sticking to the impeller and creating blood clots.

In preferred embodiments, portions of both the cage 213 and the impeller 217 comprise a non- thrombogenic surface texture with, for example, a Ra value of less than 50 nanometers.

Catheters 203 of the invention are particularly well suited for intravascular treatments on account of their non-thrombogenic properties. In certain aspects, catheters 203 of the invention include non-thrombogenic surface textures having a Ra value of less than 50 nanometers. The non-thrombogenic surface texture inhibits and/or prevents thrombosis by inhibiting the adherence of platelets and blood proteins onto surfaces of the catheter 203 when the catheter 203 is inserted into a patient's vein. In other aspects, the non-thrombogenic surface texture inhibits and/or prevents thrombosis by reducing shear forces acting on blood particles flowing through the catheter 203 since a smooth surface is less likely to shear a particle, such as a blood cell, than a rough surface.

The non-thrombogenic surface texture of devices of this disclosure may be formed by processing a metal. Processing a metal may include one or more of sanding, tumbling, polishing, electropolishing, grinding, lapping, or abrasive blasting, for example, see, Chapter 82 - Metal Processing and Metal Working Industry, Encyclopedia of Occupational Health and Safety 4th Edition, which is incorporated by reference. Preferably, the metal is processed by electropolishing, for example, as described in Cutchin, 2015, Electropolishing applications and techniques, The Tube & Pipe Journal, incorporated by reference. For example, a surface texture with a Ra of less than 50 nanometers may be generated by obtaining a piece of metal and rubbing abrasive particles against the surface of the metal to create a random, non-linear surface texture with a Ra of less than 50 nanometers. Different abrasive media may be used. A size of the cutting grains is generally referred to as “grit”, and the higher the grit number, the smaller and finer the particles are and hence the finer the surface finish they are able to achieve. Preferably, a higher grit number is used to achieve a smooth surface.

Because devices of the invention are more efficient than other devices and pump blood without initiating thrombosis, devices of the invention are beneficial for treating patients with edema. As such, in some aspects, the invention provides a method for treating edema. The method may include inserting into an innominate vein of a patient a distal portion 209 of a catheter 203 comprising an impeller assembly 211 with a cage 213 and an impeller 217 therein.

A portion of at least one of the cage 213 or the impeller 217 comprises a non-thrombogenic surface texture with a Ra value of less than 50 nanometers. Preferably, both the cage 213 and the impeller 217 comprise the non-thrombogenic surface texture. For example, in preferred embodiments, substantially all portions of the cage 213 and the impeller 217 that are exposed to blood when the distal portion 209 of the catheter 203 is inserted into the vein will comprise the non-thrombogenic surface texture. For the treatment of edema, the method includes activating the impeller 217 with, for example, a motor connected to a proximal portion of the catheter 203. Activation of the impeller 217 increases fluid flow through the innominate vein, thereby decreasing pressure at a lymphatic duct. A proximal portion of the cage 213 may be shaped to facilitate flow into an inlet 219 without recirculation or adherence of blood proteins to surfaces of the cage 213. Additionally, as discussed herein, the catheter 203 may include other features (e.g., coatings, materials, designs) that prevent or inhibit thrombosis by inhibiting adherence of blood clotting factors to surfaces of the catheter 203 or reducing shear forces. In some embodiments, methods of the invention further include the step of preparing a catheter 203 for treating edema by, for example, processing a metal. The metal may comprise one of the cage 213 or the impeller 217. Processing may involve one of sanding, tumbling, polishing, electropolishing, grinding, lapping, or abrasive blasting, the metal such that a portion of a surface of one or both of the cage 213 and the impeller 217 have a surface Ra of less than 50 nanometers, for example, 25 nanometers.

The non-thrombogenic surface texture may comprise an average depth of roughness (Rz) of less than 175 nanometers. Rz is the average distance between the highest peak and the deepest valley in five sampling lengths, or cutoffs across a surface. Rz may be calculated by measuring vertical distance from the highest peak to the lowest valley within five sampling lengths, then averaging these distances.

In some embodiments, the invention provides a catheter 203 with an impeller assembly 217 disposed at a distal portion 209. The impeller assembly 217 comprising a cage 213 housing an impeller 217 wherein at least a portion of a surface of the cage 213 or the impeller 217 comprises a non-thrombogenic surface texture having a Rz value of less than 175 nm.

Preferably, the Rz value of the non-thrombogenic surface is less than 175 nanometers. For example, the Rz value may be less than 100 nanometers.

In preferred embodiments, the impeller assembly 211 includes an expandable member 215 attached to an exterior surface of the cage 213. The expandable member 215 may be expanded to apply a radial outward force to a blood vessel wall. The device may be shaped such that application of the outward radial force substantially fixes at least a portion of the impeller assembly 217 to a central axis of the vessel wall. Upon expansion of the expandable member 215, the expandable member 215 may occludes the vein and directs blood flow into an inlet 219 of the cage. Preferably, the expandable member is a balloon. When the expandable member 215 is inflated, a proximal portion of the expandable member 215 may help to facilitate flow into an inlet 219 of the cage 213 by funneling blood therein. Additionally, when the expandable member 215 is inflated, a distal portion of the expandable member 215 may be aligned over outlets of the cage to mitigate blood recirculation. As discussed herein, the impeller assembly 217 may include features that facilitate blood flow through the cage 213. In other aspects, the invention provides intravascular devices on which a surface of the device has been chemically modified to prevent the activation of blood defense mechanisms. The device comprises a catheter 203 dimensioned for insertion into a vein such as a jugular vein. The catheter 203 includes a proximal portion and a distal portion 209. An impeller assembly 217 may be attached to the distal portion 209 of the catheter 203, the impeller assembly 217 comprising a cage 213 with an impeller 217 rotatably disposed therein. The impeller assembly 211 may be designed to inhibit thrombosis on account of at least a portion of the cage 213 and/or the impeller 217 comprising a modified surface chemistry provided by at least one of a coating or a surface treatment. A modified surface chemistry may include a surface having a physical, chemical, or biological characteristic that different from what is found on the surface of a conventional intravascular device.

Modified surface chemistries of this disclosure may comprise a coating or a treatment. The modified surface chemistry may be a coating comprising a blood anticoagulant. For example, the coating may comprise a heparin coating such as those described in Biran, 2017, Heparin coatings for improving blood compatibility of medical devices, Adv Drug Delivery Rev 112:12-23, incorporated by reference. Heparin binds to antithrombin. Antithrombin is a serine protease inhibitor and inhibitor of blood clotting factors. Thus, in some embodiments, catheters of the disclosure display anti-thrombogenic properties on account of coatings with surfaces having an affinity for antithrombin. In some embodiments, heparin may be immobilized on a surface of the cage 213 or the impeller 217 by attaching heparin to a compatible functional group deposited on the surface of the cage 213 or the impeller 217 or by priming the surface of the cage 213 or the impeller 217 with a matrix onto which heparin may covalently bind. As an example, the coating may include pre-assembled aggregates of heparin molecules such as found in the coating sold under the trade name CHC, by Corline Biomedical AB, Sweden. In some embodiments, the coating may comprise heparin that is covalently bonded to a hydrophilic priming layer such as found in the heparin coating sold under the trade name ASTUTE by Biointeractions Ltd. Alternatively, heparin devices of the disclosure may include a release-based approach, wherein small amounts of heparin are released overtime. Alternatively, the coating may comprise warfarin, which is an anticoagulant used to reduce the formation of blood clots.

In some embodiments, the modified surface chemistry may comprise a hydrophilic coating that establishes or enhances hydrophilic properties of a surface of the catheter 203. Hydrophilic surfaces attract water and allow wetting of the surface. Hydrophilic surfaces generally have a droplet contact angle measurement of less than 90 degrees. Providing hydrophilic surfaces on portions of the catheter 203 such as at least one of the cage 213 and/or the impeller 217 is advantageous for preventing thrombosis because hydrophilic surfaces may adhere to water molecules present in blood to the exclusion of blood clotting factors. In some instances, upon inserting the catheter inside the vein, the hydrophilic surface of the cage 213 and/or the impeller 217 may create a layer of water molecules on the hydrophilic surface that functions as a barrier preventing plasma protein adherence by eliminating possible binding sites.

The hydrophilic coating may be made by treating a surface of the catheter 203 with an acid, such as hyaluronic acid, for example, as provided by the hydrophilic coating sold under the trade name Hydak, by Biocoat, Inc., Horsham, PA. In other embodiments, the coating may be made by, for example, submerging a portion of the catheter 203 in a wetting fluid. The wetting fluid may comprise a salt of an organic acid, for example, a benzoate or a sorbate, and a pH buffer. In other embodiments, the coating may comprise a hydrophilic coating such as the coating sold under the trade name Acuwet by Aculon, San Diego, California.

In some embodiments, the modified surface chemistry comprises a modified oxide layer. Oxide layers are layers formed by the reaction of a material's surface with oxygen. Modifications to the oxide layer include changes in thickness, topography, and chemical composition. Such modifications are useful for improving surface wettability which reduces adherence of blood clotting factors. In some instances, the oxide layer is formed or modified by one of electropolishing, heat treatment, or acid passivation. Preferably, the oxide layer is modified by electropolishing, also known as electrochemical polishing, anodic polishing, or electrolytic polishing (especially in the metallography field). Electropolishing is an electrochemical process that removes material from a metallic workpiece and may also be used to reduce surface roughness by levelling micro-peaks and valleys, thereby improving the surface finish. Methods of modifying the oxide layer may remove or reduce organic contaminants present on the surface of the catheter, which may further improve hydrophilicity. In preferred embodiments, the modified surface chemistry may be provided by a surface oxidation.

The modified surface chemistry may be generated by a surface oxide treatment that includes plasma electrolytic oxidation, also known as electrolytic plasma oxidation or microarc oxidation. Plasma electrolytic oxidation comprises an electrochemical surface treatment process for generating oxide coatings on metals. Plasma electrolytic oxidation includes high potentials that create discharges resulting in plasma that modifies the structure of the oxide layer. This process can be used to produce oxide coatings on metals.

In some embodiments, the modified surface may further comprises one of a metal oxide of titanium oxide (TiO), titanium dioxide (Ti02), dititanium trioxide (TΪ203), chromium (II) oxide (CrO), chromium (III) oxide (Cr203), chromium dioxide (Cr02), chromium trioxide (Cr03), chromium (IV) or any combination thereof. In some embodiments, at least one of the cage 213 or the impeller 217 comprises a modification to the oxide layer and the thickness of the oxide layer provides improved biocompatibility of the device. The thickness of the oxide layer may be, for example, less than 5000 picometers, less than 3000 picometers, less than 2000 picometers, or is greater than 200 picometers, greater than 400 picometers, or greater than 600 picometers. In some embodiments, a modification to the oxide layer comprises replacing a portion of the surface's native oxide layer with a more uniform oxide layer.

Aspects of the invention provide an indwelling catheter in which at least a portion of the cage 213 or the impeller 217 comprises a modified surface chemistry (e.g., a treatment or coating). In some embodiments, substantially all of a surface of the cage 213 that is exposed to blood when the cage 213 is positioned inside of a vein will comprise the modified surface chemistry. Substantially all generally means greater than at least 50 percent, for example, at least 75 percent of a portion of the cage 113 that is exposed to blood inside the vein. In some embodiments, portions of the cage 113 comprising inlets 219 and outlets 221 will comprise the modified surface chemistry as these portions may be particularly prone to thrombosis due to fluid flow patterns that may exist such as recirculation. In some embodiments, inner surfaces of the cage 113 that contact blood will comprise the modified surface chemistry.

In some embodiments, portions of the impeller 217 may comprise the modified surface chemistry. For example, greater than at least 50 percent of the impeller 217 that is exposed to blood when the catheter 203 is inside the vein may comprise the modified surface chemistry. Preferably, both of the cage 213 and the impeller 217 comprise the modified surface chemistry in order provide the greatest protection against thrombosis.

In some embodiments, one or more portions of at least one of the cage 213 and/or the impeller 217 comprises a surface texture having a Ra value of less than 50 nanometers in addition to a modified surface chemistry. Preferably, portions comprising the surface texture and the modified surface chemistry overlap such that some areas of the cage 213 and/or the impeller 217 include both a surface texture having an Rz value of less than 150 nanometers and a modified surface chemistry such as a coating or treatment that may increase hydrophilicity. The modified surface chemistry may follow the contours and roughness of the cage 213 or the impeller 217. In some embodiments, the modified surface chemistry comprises a coating thickness and the coating thickness is greater than the Rz of the surface of the cage 213 or the impeller 217.

In preferred embodiments, the modified surface chemistry is provided on portions of the cage 213 and/or the impeller 217 and provides a hydrophilic surface comprising a water contact angle of 20 degrees or less, for example, the surface may comprise a water contact angle of 10 degrees or less. The water contact angle is the angle that a droplet of water creates with a solid (e.g., the cage 213 or impeller 21) when the water droplet is deposited on the solid. In some embodiments, the modified surface chemistry comprises a super-hydrophilic surface. A super- hydrophilic comprises a static contact angle of less than 10 degrees and may have a rolling-off angle of greater than 10 degrees. The roll-off angle is the angle of inclination of a surface at which a drop rolls off. The super-hydrophilic surface may be generated by modifying an oxide layer of the surface of the cage 213 or the impeller 217.

In some embodiments, the modified surface chemistry comprises a hydrophilic functional group. Functional groups are groups of chemicals that are attached to carbon atoms in the place of hydrogen atoms and hydrophilic functional groups are functional groups that are "water loving", i.e., hydrophilic in nature. For example, the hydrophilic functional group may comprise one or more of a hydroxy group, a carboxyl group, an amine group, a carbonyl group, a chloro group, an ether group, or a phosphate group.

The modified surface chemistry may comprise a coating. Preferably, the coating comprises at least one of a polysaccharide, a polymer, or a hydrogel. The coating may further comprise one or more of a polyurethane, polyethylene glycol, poly-2-oxazolines, polyvinyl alcohol, polyvinylpyrrolidone, maleic anhydride copolymer, poly(lactide-co-glycolide), aminoalkyl(meth)acrylamide, aminopropylmethacrylamide, copolymers and blends of the aforementioned. In some instances, the coating further comprises one of polyethyleneimine, polyurethane, a sulfonate group, albumin, a polyamine, polyvinyl siloxane, hyaluronic acid, or any combination thereof. In some embodiments, the modified surface chemistry may comprise a coating comprising a polysaccharide. Preferably, the polysaccharide comprises heparin. Heparin, also known as unfractionated heparin, is a medication and naturally occurring glycosaminoglycan. Heparin decreases the clotting ability of the blood. Coating a surface of the catheter, such as a portion of at least one of the cage 213 or the impeller 217, may reduce risks of blood clots as well as catheter-related blood stream infections and bacterial colonization of the catheter 203.

Devices of the invention may minimize risks of thrombosis formation by incorporating non-thrombogenic materials. As used herein, a non-thrombogenic material is a material having minimal thrombogenic affects when inserted into a blood stream. According to some aspects of the disclosure, intravascular devices are provided comprising a catheter 203 dimensioned for inserting into a vein, such as a jugular vein. The catheter 203 comprising a proximal portion and a distal portion 209; and a cage 213 attached to the distal portion 209 of the catheter 203, the cage 213 housing an impeller 217, wherein a portion of a surface of the cage or the impeller comprises a non-thrombogenic metal. In some embodiments, the non-thrombogenic metal is, for example, titanium. Preferably, the non-thrombogenic metal includes an oxide layer modification that renders the surface highly hydrophilic. Preferably, the modification improves uniformity of the oxide layer. The oxide layer may be modified by a treatment. For example, the treatment may comprise one of electropolishing, heat treatment, or acid passivation. The treatment may comprise a surface oxidation treatment that removes and generates new oxide layers.

Preferably, at least one of the cage 213 or the impeller 217 comprises the non- thrombogenic metal. In some embodiments, the cage 213 comprises the non-thrombogenic metal. For example, in some embodiments, substantially the entire surface of the cage 213 or the impeller 217 that is in contact with blood when the catheter is inside the vein has the non- thrombogenic metal.

The non-thrombogenic metal may comprise a transition metal or a post-transition metal. Transitional metals are any of the set of metallic elements occupying a central block (i .e, groups IVB-VIII, IB, and IIB, or 4-12) in the periodic table, e.g., iron, manganese, chromium, and copper. Post transition metals, also known as the poor metals, are a group of metals on the periodic table, positioned the right of the transition metals. The group 12 elements may be included. Germanium, antimony, and polonium also may be included. Preferably, the non- thrombogenic metal comprises one of titanium, cobalt, nickel, zirconium, gold, silver, or iridium, aluminum, tin, gallium, stainless steel, or nickel titanium. The non-thrombogenic metal may be selected on account of its hydrophilic properties that inhibit blood clots while the catheter is inside the vein.

In preferred embodiments, devices of the invention include non-thrombogenic metals comprising one or more of a non-thrombogenic surface texture and/or non-thrombogenic modified surface chemistry as described herein. In some embodiments, the cage 213 and/or impeller 217 comprise a surface layer and the surface layer comprises an enriched concentration of titanium or chromium.

In some aspects, the invention provides an intravascular device useful for treating medical conditions such as edema. The device comprises a catheter 2003 dimensioned for insertion into a vein. The catheter 203 comprises a proximal portion and a distal portion 209; a cage 213 attached to the distal portion of the catheter 203; and an expandable member 215 attached to an exterior surface of the cage 213, wherein a portion of a surface of the expandable member 215 is non-thrombogenic, i.e., comprises properties that reduce thrombosis.

In some embodiments the non-thrombogenic surface of the expandable member 215 comprises a block copolymer comprising a first polymeric block and a second polymeric block.

A block copolymer is a copolymer formed when, for example, two monomers cluster together and form 'blocks' of repeating units. For example, a polymer made up of X and Y monomers joined together like: -Y-Y-Y-Y-Y-X-X-X-X-X-Y-Y-Y-Y-Y-X-X-X-X-X- is a block copolymer where -Y-Y-Y-Y-Y- and -X-X-X-X-X- groups are the blocks. In some preferred embodiments, a polymeric block comprises a hydrophilic functional group. Hydrophilic functional groups may include ether groups, amine groups, urethane groups, urea groups, ester groups, hydroxyl groups, carbonyl groups, carboxyl groups, amino groups, sulfhydryl groups, or phosphate groups. In another preferred embodiment the polymeric block comprises functional groups that confer rigidity to the block. Functional groups conferring rigidity may be aromatic or aliphatic. Functional groups conferring rigidity may include groups that comprise a ring structure. These ring structured groups may be aromatic or aliphatic. The hard block may comprise a mix of ring structure groups and linear groups. Linear groups may include amine groups, urethane groups, urea groups, carbonate groups and methylene groups. A second polymeric block may comprise a polymer repeat unit selected to enhance flexibility in the second polymeric block. The second block may comprise a polyether, a polyester, a polycarbonate, a polybutadiene, a poly dimethyl siloxane or a mixture of these. The first and second polymeric blocks may be substantially immiscible and when copolymerized form phase separated blocks within a polymer matrix. The phase separation may be manifested on a surface of said expandable member 215.

In some instances, the polymer may comprise non-bound chemical species, the non-bound chemical species comprising oligomers and additives. The polymer may be treated so as to remove non-bound chemicals and further manifest the phase separation on the surface of the expandable member 215. Moreover, by removing the non-bound chemicals, hydrophilicity of the surface may be improved.

The non-thrombogenic surface of the expandable member 215 may comprises a hydrophilic coating and/or a hydrophilic material. When inside a vein, the hydrophilic coating or hydrophilic material of the expandable member 215 may bind to water molecules to the exclusion of blood plasma proteins, thereby preventing blood clots. In some embodiments, the surface of the expandable member 215 includes one or more portions with the hydrophilic coating and portions without the hydrophilic coating. The one or more portions with and without the hydrophilic coating may form a pattern, the pattern may be more apparent when the expandable member 215 is in an expanded state. The pattern may increase the non-thrombogenic properties of the surface of the expandable member 215 and further help to reduce blood clotting. The pattern may, for example, improve non-thrombogenic properties of the device by disrupting blood clotting factors from adhering to portions of the catheter including the expandable member 215. For example, the pattern may comprise stripes, spirals, waves, or may be a zebra pattern.

The hydrophilic coating may comprise one of a polysaccharide, a polymer, or a hydrogel. Polysaccharides are long chains of carbohydrate molecules, specifically polymeric carbohydrates composed of monosaccharide units bound together by glycosidic linkages. In preferred embodiments, the polysaccharide comprises heparin. In some embodiments, the expandable member 215 comprises a polymer, the polymer comprising silicon.

Aspects of the invention provide a catheter 203 comprising an expandable member 215. The expandable member 215 includes features such as materials and coatings that inhibit thrombosis. Preferably, the expandable member 215 comprises hydrophilic materials. For example, the material may comprise one of polyethylene terephthalate, polyamide, polyurethane, or nylon. Preferably, the expandable member 215 comprises polyurethane. In some embodiments, the expandable member 215 further includes a hydrophilic coating. The hydrophilic coating may comprises more than half of the surface of the expandable member 215 that is exposed to blood when the expandable member is in an expanded state inside the vein. In some embodiments, the expandable member 215 comprises a hydrophilic coating on a proximal portion and/or a distal portion, which may align with inlets 219 and outlets 221 of the catheter 203 when the expandable member 215 is in a deployed state.

Preferably, the expandable member is a balloon, and upon expansion of the balloon inside a vein, the balloon opposes a wall of the vein and helps direct blood flow into an inlet 219 of the cage 213. Moreover, upon expansion of the balloon, a distal-most portion of the balloon may be aligned over the inlets 219 or the outlets 221 to mitigate blood recirculation. Mitigation of blood recirculation may further reduce thrombogenicity of the device by minimizing shear forces acting on blood particles.

FIG. 3 shows an inlet 319 of an impeller assembly. The inlet 319 is defined by a plurality of struts 331. One or more of the struts 331 may comprise an inflation lumen (not shown) that connects to an expandable member and may be used to, for example, deliver fluid to the expandable member for inflation.

FIG. 4 shows an outlet 421 of an impeller assembly. The outlet 421 is at least partially defined by a plurality of struts 431 and at least partially aligns with an impeller 417 disposed within the impeller assembly. An angle of the impeller 417 extends upwards towards a proximal portion of the impeller assembly. The upward angle of the impeller 417 provides a surface that guides a flow of fluid exiting the impeller assembly. In particular, the surface is optimized so as to facilitate the flow of fluid from the impeller assembly such that the fluid experiences minimal to no disturbances in flow such as vortices.

FIG. 5 shows a portion of a cage 513 comprising an inlet 519 with a non-thrombogenic surface finish. In particular, the cage 513 comprises a metal and portions of the metal have been processed by, for example, electropolishing such that the cage 513 has non-thrombogenic surface finishes. Portions of the cage 513 having the non-thrombogenic surface finish include the inlets 519. The cage 513 further includes a rough surface 533 formed by, for example, etching. The rough surface may be provided for an improved interfacial adhesion between an expandable member and the cage 513.

FIG. 6 shows an impeller 617. As described herein, the impeller 617 may be disposed within an impeller assembly and connected to a motor by a flexible drive cable 637 that extends through the catheter connecting the motor to the impeller. The drive cable 637 may comprise a metal such as nickel -titanium alloy, i.e., nitinol, selected for its biocompatibility, kink resistance, and elasticity properties. The drive cable 637 may comprise a non-thrombogenic surface texture having a Ra value of 75 nanometers or less, preferably 50 nanometers. In some instances, the drive cable 637 comprises a polyether ether ketone (PEEK) liner for providing biocompatibility and reduced friction. The impeller 617 comprises at least one blade 639. The impeller blade 639 is configured to be in fluidic engagement with the impeller assembly (refer to FIG. 2) such that the impeller 617 may rotate in clearance with an inner lumen of the impeller assembly 211 during operation. Blade clearance may be, for example, between 7-110 micrometers. A radial dimension of the impeller blade 617 may vary across a proximal portion and distal portion of the impeller 617.

FIG. 7 shows an impeller assembly 711 with an expandable member 715. The expandable member 715 is shown in an inflated configuration. Preferably, the expandable member comprises a balloon. For example, in preferred embodiments, the expandable member 715 comprises a polyurethane balloon. As discussed herein, the balloon 715 may comprise a coating that provides hydrophilic properties. At is distal end of the impeller assembly 711 is an atraumatic tip 741. The atraumatic tip 741 preferably comprises a soft material such as a polymer. The material may include, for example, a polyether block amide, such as those sold under the trademark PEBAX by Arkema Inc. (King of Prussia, PA).

FIG. 8 shows a distal view of an impeller assembly 817. The impeller assembly 817 includes an expandable member which is shown in a transparent form. An inflation lumen 843 extends along an outer surface of the impeller assembly 817 for inflating the expandable member. The inflation lumen 843 may, for example, be used to deliver a fluid to the expandable member thereby causing the expandable member to inflate. A biologically inert fluid such as saline may be used to inflate the expandable member by way of the lumen since saline does not react with the body and is relatively safe in the event that one of the lumen or the expandable member leaks during operation.

FIG. 9 shows an impeller 917. The impeller may include an optimized blade impact angle 918 to reduce negative axial velocity (recirculation) of fluid traveling through the cage in which the impeller is housed. For example, the optimized blade impact angle may comprise an inclined or tapered surface disposed at a proximal end of the impeller blade 939. A proximal end of the impeller 917 may be spaced apart from a distal end of a cuff 947. The proximal end of the impeller 917 and the distal end of the cuff 947 may define a gap (not shown). In preferred embodiments, the gap comprises one of a non-thrombogenic surface texture or coating, as discussed above, in order to prevent blood particles such as proteins and platelets from adhering to gap surfaces and creating clots.

FIG. 10 shows an inlet region 1019 of a cage 1013 with a cuff removed. The cage 1013 comprises reservoirs 1049, for example, 5-6 small holes around a proximal part of the cage 1013. During manufacturing, the reservoirs 1049 may be filled with an adhesive to bond the cage 1013 to the cuff on the proximal side. The adhesive seals up the reservoirs and provides a smooth and biocompatible surface finish. Exemplary adhesives include low viscosity cyanoacrylates and ultraviolet cure adhesives. A similar approach may be employed to bond the cage 1013 to a bearing housing, or catheter tip, on the distal side, as discussed below.

In some embodiments, catheters of the invention further include one or more sensors that are in operable communication with an expandable member attached to an outer surface of a cage of an impeller assembly. The one or more sensors may be disposed on the catheter, for example, on the impeller assembly near an inlet and/or an outlet. The sensors, for example, pressure sensors, may be used sense a pressure change in a vein in which the catheter is inserted. The pressures sensors may be configured to detect changes in pressure and based on detected changes in pressure, may provide data that is used to regulate a flow of fluid through the impeller assembly by adjusting a rotational velocity of an impeller disposed therein, the sensors may provide data that is used to adjust a size or shape of the expandable member by, for example, sending data to a computer that processes the data and sends instructions to an automated syringe pump to inflate the expandable member with a fluid such as saline.

With reference to FIG. 2, in preferred embodiments, the catheter 203 further comprises a cuff 249 attached to a proximal portion of the cage 213, the cuff 249 provides a smooth transition between an outer surface of the catheter 203 and a proximal portion of the cage 213. In some instances, the cuff 249 may comprise a non-thrombogenic surface texture having, for example, an Ra value of 50 nanometers or less, such as 25 nanometers. Alternatively, or in addition to, the cuff 249 may comprise a modified surface chemistry, as discussed above, with, for example, a coating or treatment that enhances hydrophilic properties of a surface to preferentially adhere water molecules to the exclusion of blood proteins. Moreover, the cuff 249 may also comprise a non-thrombogenic material, such as, for example, titanium, and may comprise a surface oxidation treatment that removes and generates a new surface oxide layer.

In some embodiments, a bearing assembly 251 is disposed at a distal portion of the impeller assembly 211. The bearing assembly 251 comprising a housing 253 with one or more bearings 257 disposed therein. Preferably, the housing 253 comprises titanium. The bearings 257 may be, for example, ceramic bearings. The bearings 257 provide important benefits to the catheter 203 by reducing friction generated by the rotational movement of the impeller 217 during operation. The bearings 257 may allow the impeller 217 to rotate more freely. The bearing housing 253 may comprise PEEK, or a metal such as titanium, and may further comprise a non-thrombogenic surface texture or modified surface chemistry such as a coating and/or treatment, as described herein, to prevent thrombosis while inside a blood vein. In some embodiments, a distal gap 263 is defined by a portion of the bearing assembly 251, or catheter tip, and the impeller 217. The distal gap 263 may be, for example, greater than 20 micrometers and less than 60 micrometers. The distal gap 263 may be configured so as to allow the impeller 217 to rotate efficiently without trapping blood proteins therein. To that end, the distal gap 263 may comprise a non-thrombogenic surface texture or modified surface chemistry such as a coating and/or treatment, as described herein. For example, surfaces of the impeller 217 and/or bearing assembly 251 which define the distal gap 263 may comprise a surface texture having a RA value of less than 50 nanometers or may comprise a treatment that modifies an oxide layer of the surface as discussed herein.

A proximal gap 265 may be located at the proximal portion of the impeller assembly 211. The proximal gap 265 may be defined by a portion of the cage 213 and a proximal portion of the impeller 217. The proximal gap 265 may be designed so as to allow the impeller 217 to rotate efficiently without trapping blood proteins therein. To that end, the proximal gap 265 may comprise a non-thrombogenic surface texture or modified surface chemistry such as a coating and/or treatment, as described herein. For example, surfaces of the impeller 217 and/or cage 213 which define the proximal gap 265 may comprise a surface texture having a RA value of less than 50 nanometers or may comprise a surface oxidation treatment.

Preferably, the cage 213 is substantially cylindrical in shape. The cage 213 may be configured to facilitate a flow of fluid through an interior lumen 261 such that the flow experiences minimal disturbances in flow patterns such as vortices and recirculation. In particular, the cage 213 may be designed so as to include stepped portions that define changes in inner diameters within the cage 213 and manipulate the flow of fluid therein. In some embodiments, for example, as shown in FIG. 2, the lumen 261 of the cage 213 is narrower at a proximal portion than at a distal portion to increase flow rate of fluid traveling through the cage 213. In other embodiments, the lumen 261 of the cage 213 may taper towards, for example, the distal end. In some embodiments, the cage 213 comprises an outer wall that is thicker at a proximal portion than at a distal portion of the cage 213.

This disclosure provides a catheter comprising a cage. Preferably the cage houses an impeller and at least part of the cage or the impeller has a thrombogenic resistant surface texture. The surface texture of the cage or impeller may be resistant to thrombosis formation on account of its smooth surface. In particular, any surface interstices (e g., crevices, gaps, spaces) present on the cage or the impeller are made smaller than potentially adherent plasma proteins thus establishing a surface environment on which the plasma proteins struggle to grip the surface.

FIG. 11 shows an exemplary cage 1113. The cage 1113 is designed to be attached to a distal portion of a catheter and may be dimensioned for insertion into a vein or an artery. Preferably, the cage 1113 houses an impeller for facilitating a flow of blood through the cage 1113 when operating inside the vein or artery.

FIG. 12 shows a scanning electron microscope image of a surface of a conventional metal cage at high magnification. An inclusion 1251 or material defect is shown on the surface. Depending on a size or profile of the inclusion 1251, the inclusion 1251 may impart a local roughness that promotes thrombus formation. The roughness may promote thrombus formation by presenting a gripable surface onto which a blood clotting protein, e.g., fibrinogen, may adhere.

One insight of the invention is that surface roughness may be manipulated so as to influence the types of particles, such as plasma proteins, that may or may not be adsorbed onto the surface. Such manipulations may be useful for inhibiting thrombosis formation. For example, if the surface roughness, as measured by Ra, is small relative to a particular plasma protein, e.g., fibrinogen, then that plasma protein is less likely to be adsorbed onto the surface. However, smaller (and in some instances more abundant) plasma proteins, e.g., albumin, may be adsorbed if the smaller plasma protein is smaller than any interstices provided by the roughness profile. Albumin adsorption is not associated with a harmful thrombosis response. By modulating the Ra of the surface, a surface may be designed to preferentially associate with proteins less likely to illicit harmful blood clots such as albumin. FIGS. 13 and 14 highlight this principle.

FIG. 13 shows plasma proteins 1361 and interstices 1365 of a surface 1371 with a Ra of 800 nanometers. Because of the interstices 1365 are relatively larger than the plasma proteins 1361, the plasma proteins 1361 can easily get lodged and grip the surface 1371. In instances where the plasma protein is, for example, fibrinogen, adherence or association of the protein may result in thrombus formation.

FIG. 14 shows plasma proteins 1461 and interstices 1465 of a surface 1471 with aRa of 50 nanometers. Because of the interstices 1465 are relatively smaller than plasma proteins 1461, the plasma proteins 1461, such as fibrinogen, find it more difficult to anchor onto the surface 1471. If the surface chemistry is benign then this effect may be even more pronounced. Thus, it is evident that plasma proteins can more easily anchor to the interstices of the 800 nanometer surface (FIG. 13) whereas the 50 nanometer surface does not promote anchoring of plasma proteins in surface interstices.

Table 1, below, presents information relating to blood proteins and thrombosis.

These data show albumin is abundant and relatively small in size, whereas fibrinogen is less abundant and much larger in size. Since, fibrinogen adsorption can cause formation of blood clots, cages and impellers having surface textures within the scope of this disclosure may comprise a roughness profile with interstices too small for a protein as large as fibrinogen to adhere, but may, in some instances, allow smaller proteins such as albumin to adhere. Since albumin is not associated with blood clots, it may be advantageous to permit the binding of albumin, as the presence of harmless blood proteins such as albumin may further prevent (for example, by steric hindrance) associations with blood proteins that may illicit harmful blood clots. Thus, the invention may provide a surface texture in which interstices of the surface are too small for fibrinogen to adhere, but in some instances, may allow smaller abundant proteins such as albumin to adhere.

In addition, there are a number of globulins in blood plasma including g-globulin which is relevant in thrombosis. The globulin g-globulin is relatively large with a 32 nanometer max linear dimension. Preferably, interstices present on cages and impellers of the disclosure are too small for g-globulin to be adsorbed onto the surface. Von Willebrands factor is much less abundant protein but an important protein in thrombus formation. This protein is large and is broken up into smaller functional proteins by shear stress. It is thus difficult to call out a dimension for this protein as its size is environment dependent. Although, within preferred embodiments, surfaces of cages and/or impellers may comprise a roughness profile with interstices that are too small for a von Willebrands factor to adhere.

FIG. 15 shows a metal substrate 1501 with a modified surface chemistry 1507. The modified surface chemistry 1507, as described above, may be designed to attract and bind with water molecules 1509. The binding of water molecules 1509 to the modified surface 1507 may form a barrier layer 1511 that prevents the adsorption of plasma proteins 1515 and platelets 1513 onto the surface. Such a design may prevent or reduce incidents of blood clot formation.

Specifically, catheters of the invention can include a metal interface 1500 disposed between a metal substrate 1501 and blood 1516. The metal interface 1500 (sometimes referred to as the metallic interface) relates to surfaces of catheters that, when positioned inside a blood vessel, are in contact with blood. The metal interface 1500 can include a surface layer or layers, e.g., layers of modified surface chemistry 1507, that interface between the metal substrate 1501 and blood. Illustrated are two important components of blood, plasma proteins 1515 and platelets 1513.

The adsorption of plasma proteins 1515 generally onto the surface of medical devices happens immediately on contact with blood. This plays an important role in how the body responds to the surface 1500 of the medical device over time. Plasma protein adsorption is a phenomenon whereby a thin film of plasma proteins is laid onto the surface of a substrate. Since over 100 plasma proteins have been identified to date it will be appreciated that any given surface or any given segment of a surface can precipitate its own unique plasma protein response. Non-thrombogenic surfaces of the invention adsorb proteins or combinations of proteins that mark these surfaces as more benign whereas thrombogenic surfaces adsorb proteins or combinations of proteins that mark these surfaces as more foreign. Platelets 1513 are multifunctional blood cells and they play a central role in the development of thrombus.

According to one preferred embodiment, the modified surface chemistry 1507 is designed such that the surface can generate a benign response from plasma proteins. In another embodiment, the modified surface chemistry 1507 is designed to attract benign plasma proteins like albumin. In yet another embodiment the modified surface chemistry 1507 is established such that the surface can bind to water so as to prevent plasma protein adsorption onto the metal interface 1500.

The modified surface chemistry 1507 can involve an enhanced oxide layer. The enhanced oxide layer may include a passivation of the surface 1500. The enhanced oxide layer may involve the exclusion or removal of undesirable oxides from the surface. Undesirable oxides can be removed through electropolishing, for example. The enhanced oxide layer may involve a modification of a spontaneously formed oxide layer to increase the hydrophilicity of the layer.

The modified surface chemistry 1507 may include a first layer 1520 and a second layer 1521, the second layer 1521 being disposed or laid down on top of the first layer 1520. In this embodiment the first layer 1520 can include an oxide film extending over the metal surface 1500, e.g., the metallic interface of the cage 1013 and/or impeller 939. The second layer 1521 may include a polymer layer 1522. The polymer layer 1522 may include a hydrophilic polymer. The polymer layer 1522 can have a hydrophilic polymer with a thickness of less than 5,000 nanometers, for example, 4,000, or 3,000, or 2,000 nanometers. A reduced polymer thickness can be useful to minimize or prevent instances of mechanical interference, especially when polymer 1522 is disposed in the gap region between the cage and the rotating impeller. In one embodiment the polymer layer 1522 is formulated for binding to water molecules. The ability of the polymer layer 1522 to bind to water can be measured using a contact angle measurement, as known in the art. Preferably the polymer layer 1522 generates a water contact angle of less than 20 degrees. In another embodiment the polymer layer 1522 is configured to generate a water contact angle of less than 10 degrees.

In one embodiment the polymer layer 1522 can include a plurality of polymer chains 1523. The plurality of polymer chains 1523 each having a hydrophilic end 1524 and a binding end 1525. The binding end 1525 is formulated to bond to the first layer 1520 of modified surface chemistry 1506 and the hydrophilic end 1524 is designed to interact strongly with water molecules. In one embodiment the binding end 1525 of the plurality of polymer chains 1523 is hydrophobic. In one embodiment the binding end 1525 of the plurality of polymer chains 1523 is designed to establish strong van der Waals attractive forces with said first layer 1520.

In one embodiment the binding end 1525 of the plurality of polymer chains 1523 is designed to establish strong polar attractive forces with said first layer 1520. In one embodiment the binding end 1525 of the plurality of polymer chains 1523 is designed to establish strong van der Waals and polar attractive forces with the first layer 1520. The strong intermolecular attractive forces of the binding region 1525 of the polymer chains 1523 binds the unbound hydrophilic end 1524 to the first layer 1520. The unbound hydrophilic chain ends 1524 are designed to be independent of each other. In one variation the unbound hydrophilic chain ends 1524 includes a linear polymer. In another variation, the unbound hydrophilic chain ends 1524 includes a branched polymer. In one embodiment, the binding end 1525 of the plurality of chains 1523 includes a plurality of linear polymer chains. In another embodiment, the binding end 1525 of the plurality of chains 1523 is designed to interpenetrate with adjacent binding chain ends.

The plurality of polymer chains 1523 can include a block copolymer in another embodiment with one block having a hydrophilic bock and the second block having a binding block. In one embodiment the polymer layer 1522 includes a phosphoryl choline polymer. In another embodiment, the polymer layer 1522 includes a polyethylene oxide polymer. In another embodiment, the polymer layer 1522 includes a polyethylene succinate polymer. In another embodiment, the polymer layer 1522 includes a polyethylene adipate polymer. In another embodiment, the polymer layer 1522 includes a poly(vinyl alcohol-co-ethylene) polymer. In another embodiment, the polymer layer 1522 includes a polyacrylic acid polymer. It will be appreciated that based on the above disclosure that the polymer layer 1522 may include mixtures or copolymers of the aforementioned polymers or block copolymers or other polymers, such as hydrophobic polymers commonly used in the art.

FIG. 16 shows a subset of elements in the periodic table with electronegativity (EN) values below each element. For example, hydrogen has an EN value of 2.2. Aspects of this disclosure provide a surface of a catheter with a modified surface chemistry. The modified surface chemistry may comprise atom pairs with an EN difference of at least 0.8, and preferably at least 1.2, or greater. For example, the modified surface chemistry may have a high concentration of hydroxyl (-OH) groups. The difference between the EN values for H and O is [3.44 - 2.2 = 1.24] A modified surface chemistry that is rich in atom pairs with an EN difference of 1.24 will confer hydrophilic properties to the surface of the metal. Accordingly, elements preferred for use with catheters of the invention are identified by dark circles 1603. The greater the concentration of hydroxyl groups, or atom pairs with similar EN differences on the surface, the more strongly water will compete (and displace) plasma proteins for adsorption onto the surface. Water successfully displacing plasma proteins on the surface pacifies the surface in terms of thrombus formation - even in high shear conditions or conditions of recirculation or conditions of blood stasis.

FIG. 17 shows a schematic stress strain curve for an elastomer suitable for making an expandable member according to aspects of the invention. The top curve 1750 represents the stress strain curve for the elastomer as it is stretched in tensile. The lower curve 1760 is the stress strain curve for the elastomer as it is allowed to relax from a max test strain 1770. The area between the two curves (Area A) is a measure of the energy loss in the cycle of stretching and then un-stretching the material. The hysteresis loss ratio is the ratio of area A divided by areas A+B all expressed as a percentage. Where the percentage hysteresis loss ratio is low then the material will have desirable recovery characteristics. In preferred embodiments, expandable members of the invention will comprise elastomers having low hysteresis loss ratios.

FIG. 18 shows an exemplary impeller assembly 1800 comprising a cage 1817 with an expandable member 1807 attached to an outer surface in a collapsed state. The impeller assembly 1800 includes an atraumatic tip 1801 at a distal end. At a proximal end, the impeller assembly 1800 is connected to a catheter shaft 1819. The impeller assembly 1800 further includes a distal interstitial surface 1805 and a proximal interstitial surface 1809. The distal and proximal interstitial surfaces 1805, 1809 are disposed underneath the expandable member 1807 and may provide surfaces for attachment of the expandable member 1807.

In some instances, the atraumatic tip involves a bull nosed tip. For example, the tip may be approximately 3.0±1.0 mm in length having a full-spherical radius of curvature, similar to a bull-nose shape. The bull-nosed tip can be made of, for example, approximately 30-40 durometer polyether block amide loaded with a radiopaque material for improved visualization on a radiograph during insertion. The atraumatic tip may include a metallic tip, for example, the tip may include the metal of the cage. The atraumatic tip comprises a polymer tip. The polymer tip may include an elongate flexible member. The polymer tip may include a pig tail, i.e., a pig-tail shaped end. The atraumatic tip may include an elongate member of increasing flexibility.

FIG. 19 shows an exemplary impeller assembly 1900 comprising a cage 1917 with an expandable member 1907 attached to an outer surface. The expandable member 1907 is illustrated in an expanded configuration.

FIG. 20 shows an alternative embodiment of an expandable member 2007 attached to an impeller assembly 2000. In this embodiment, the expandable member 2007 folds into the collapsed state. The expandable member 2007 comprising a fold 2009 is shown.

FIG. 21 shows an expandable member 2107. The expandable member 2107 is shown in an as formed state before it is collapsed for delivery.

FIG. 22 shows a surface roughness characterization of a portion of a cage onto which a membrane may be attached. The surface is preferably an interstitial surface. The membrane may comprise a portion of an expandable member and/or facilitate the attachment of the expandable member to the cage. The roughness may provide a multiplicity of asperities and/or a plurality of interstices for attachment of the membrane. Attachment may comprise interpenetration of some of the material of the membrane around the asperities of the interstitial surface and into the interstices of the interstitial surfaces. The surface has a Ra value of 3 micrometers when measured using a laser scanning microscope. Preferably, the surface onto which the membrane and/or expandable member attaches comprises a Ra value of at least 1 micrometer, for example,

3 micrometers.

FIG. 23 shows a surface roughness characterization of a portion of a cage onto which a membrane may be attached. The membrane may comprise a portion of an expandable member and/or facilitate the attachment of the expandable member to the cage. The surface has a Ra value of 9 micrometers when measured using a laser scanning microscope.

FIG. 24 shows a standard microscopy image of a surface of a cage 2513. An interstitial area 2510 of the surface is shown between highly polished blood contacting surfaces 2540. The interstitial area 2510 preferably comprises a roughness characterized by a Ra value of between 1 and 10 micrometers. The roughness facilitates the attachment of an expandable member.

FIG. 25 shows a portion of the periodic table of elements. 2501 refers to the period 4 transition metals. 2511 identifies a group of preferred elements for use with catheters of the invention. This group of metals starts with scandium at 21 on the periodic table and ends with zinc at 30 on the periodic table. 2507 refers to the entire group of transition metals from group 3 to group 12 of the periodic table. 2509 refers to period 5 and 6 of the table.

FIG. 26 illustrates a cross sectional view of a portion of a metallic body comprising a cage or an impeller. The metallic body 2601 includes a surface chemistry that offers non- thrombogenic properties. The surface chemistry may comprise a surface film 2605. The metallic body 2601 has a metallic structure that is preferably a crystalline structure, for example, of titanium 2607. Preferably, the surface film 2605 comprises a thin surface layer comprising an oxide with at least one of the metallic elements of the metallic body 2601. For example, as shown in FIG. 26, the metallic body 2601 comprises titanium and the oxide film also comprises titanium. In another embodiment the surface film 2650 comprises a thin surface layer composed of a first metal oxide and a second metal oxide. In one variation of this embodiment the first metal oxide comprises a titanium oxide and the second metal oxide comprises an aluminum oxide. In another variation of this embodiment the first metal oxide comprises a chromium oxide and the second metal oxide comprises a nickel oxide. In another variation of this embodiment the first metal oxide comprises a chromium oxide and the second metal oxide comprises a cobalt oxide. FIG. 27 shows a schematic of a lattice structure 2700 of a surface film 2705. The surface film 2705 is a titanium oxide film. It will be appreciated that a number of other oxide films are possible including chromium oxide and aluminum oxide. In at least one embodiment, the lattice structure comprises a reutile-like lattice structure. Rutile is a mineral composed primarily of titanium dioxide (Ti02), and is the most common natural form of Ti02. Other polymorphs of Ti02 may also be used, including anatase, akaogiite, and brookite.

In one aspect, the invention provides an intravascular device including a catheter dimensioned for insertion into a vein. The catheter having a proximal portion and a distal portion and a cage attached to the distal portion of the catheter, the cage housing an impeller. At least a portion of the surface of the cage or the impeller having a non-thrombogenic metallic interface. The non-thrombogenic metallic surface includes non-thrombogenic metals, as discussed herein, which are intended to be in contact with blood when the catheter is in use inside the vein.

The non-thrombogenic metallic interface may be a metal oxide film. The metal oxide film being formulated to confer or enhance non-thrombogenic properties of a metal of the catheter. The metal oxide film may include an oxygen active material, which is a material that spontaneously forms an oxide when exposed to oxygen without the need for a catalyst to facilitate the reaction. The oxygen active material can be a material that spontaneously forms an oxide when exposed to air or an atmosphere with a similar oxygen content to air.

The non-thrombogenic metallic interface may include a coating. The coating may be a metal oxide film. The metal oxide film can include hydrophilic groups that attract water molecules from blood, thereby displacing blood proteins associated with thrombosis formation. In some instances, the attachment of hydrophilic groups comprises a chemical modification of the oxide film. The attachment of hydrophilic groups can include a chemical attraction, an ionic attraction or a covalent bond.

The non-thrombogenic metallic interface may include a coating. The coating may include a hydrophilic coating. The hydrophilic coating can involve a plurality of polymer chains. The plurality of polymer chains may include a hydrophilic region and a substrate attachment region. The substrate attachment region may include at least one chemical functional group designed to bond with a metal surface or a metal oxide surface. The substrate attachment region may include a plurality of functional groups that in unison bond to the metal surface or metal oxide surface. The plurality of functional groups may include a polymer chain. The plurality of functional groups may include a hydrophobic polymer chain. The plurality of functional groups may include a triol. The triol may include a chain end of a hydrophilic polymer chain. The triol comprises a R- 1,1,1 triol. The plurality of functional groups may include a silane. The plurality of functional groups may include an acrylic. The substrate attachment region may include a reactive chain end where said reactive chain end is reactive to a metal or metal oxide substrate.

The coating thickness is preferably small in comparison to the gap between the impeller and the cage. For example, the coating thickness can be less than 20% of the gap between the impeller and the cage. The coating thickness can be less than 10% of the gap between the impeller and the gage. The coating thickness can be less than 5% of the gap between the impeller and the gage. The coating thickness can be less than 2% of the gap between the impeller and the gage.

FIG. 28 shows a triol coupling agent 2800. The triol coupling agent includes alcohol functional groups concentrated on one region of the coupling agent. The triol coupling agent can be included in a coating of a catheter to enhance antithrombogenic properties. In some instances, the triol may be one of a plurality of functional groups useful for attaching a non-thrombogenic coating to a metal surface or metal oxide surface of the catheter.

Incorporation by Reference

References and citations to other documents, such as patents, patent applications, patent publications, journals, books, papers, web contents, have been made throughout this disclosure. All such documents are hereby incorporated herein by reference in their entirety for all purposes.

Equivalents

Various modifications of the invention and many further embodiments thereof, in addition to those shown and described herein, will become apparent to those skilled in the art from the full contents of this document, including references to the scientific and patent literature cited herein. The subject matter herein contains important information, exemplification, and guidance that can be adapted to the practice of this invention in its various embodiments and equivalents thereof.

Claims

What is claimed is:

1. An intravascular device, the device comprising: a catheter dimensioned for insertion into a vein, the catheter comprising a proximal portion and a distal portion; and a cage attached to the distal portion of the catheter, the cage housing an impeller, the cage and/or impeller configured for contact with human blood wherein at least a portion of a surface of the cage or the impeller comprises a non-thrombogenic surface texture with an arithmetic average roughness (Ra) that is less than a linear dimension of at least one human blood plasma protein.

2. The device of claim 1 wherein the human blood plasma protein comprises an albumen, a fibrinogen, a von Willebrand factor or a g-globulin.

3. The device of claim 1 wherein the surface texture comprises an arithmetic average roughness of less than 50 nanometers.

4. The device of claim 1, wherein the cage has the non-thrombogenic surface texture.

5. The device of claim 1, wherein both the cage and the impeller have the non- thrombogenic surface texture.

6. The device of claim 5, wherein substantially all exposed surfaces of the cage and the impeller have the non-thrombogenic surface texture.

7. The device of claim 1, wherein the cage or the impeller is metal and the non- thrombogenic surface texture is generated by processing the metal.

8. The device of claim 7, wherein the processing comprises one of tumbling, polishing, electropolishing, grinding, lapping, or abrasive blasting.

9. The device of claim 1, wherein Ra is less than 25 nanometers.

10. The device of claim 1, wherein the catheter further comprises a cuff attached to a proximal portion of the cage, the cuff providing a smooth transition between an outer surface of the catheter and a proximal portion of the cage.

11. The device of claim 10, wherein the cuff comprises the non-thrombogenic surface texture.

12. The device of claim 1, wherein the device further includes an expandable member attached around an outside of the cage.

13. The device of claim 12, wherein the expandable member is a balloon.

14. The device of claim 13, wherein upon expansion of the balloon when the catheter is in the vein, the balloon occludes the vein and directs blood flow into an inlet of the cage.

15. The device of claim 13, wherein, when the balloon is inflated, a distal portion of the balloon is aligned over outlets of the cage to mitigate blood recirculation.

16. The device of claim 1, wherein the non-thrombogenic surface texture comprises an average depth of roughness (Rz) of less than 175 nm.

17. The device of claim 1, wherein a distal portion of a shaft of the impeller and a distal portion of the cage defines a gap.

18. The device of claim 13, wherein when the balloon is inflated blood flow is directed through the cage.

19. The device of claim 18, wherein blood flowing through the cage is accelerated by a geometry of the cage and the action of the impeller.

20. The device of claim 16, wherein at least one of the distal portion of the shaft or the distal portion of the cage defining the gap comprises the non-thrombogenic surface texture.

21. The device of claim 1, wherein the portion of the surface has been rendered non- thrombogenic by a treatment to reduce roughness to thereby prevent blood clotting.

22. The device of claim 20, wherein reducing surface roughness reduces local shear forces acting on blood cells passing through the catheter while the catheter is operating inside the vein.

23. The device of claim 1, wherein the device is for treating edema.

24. The device of claim 1, wherein the cage comprises an outer wall that is thicker at a proximal portion of the cage.

25. An intravascular device, the device comprising: a catheter dimensioned for insertion into a vein, the catheter comprising a proximal portion and a distal portion; and a cage attached to the distal portion of the catheter, the cage housing an impeller, wherein at least a portion of the cage or the impeller comprises a modified surface chemistry that minimizes or prevents formation of blood clots.

26. The device of claim 25, wherein the modified surface chemistry comprises a hydrophilic surface.

27. The device of claim 26, wherein the hydrophilic surface is configured to allow blood water to outcompete blood proteins for adhesion with the surface when the catheter is inserted into the vein.

28. The device of claim 27, wherein the hydrophilic surface is configured to preferentially adhere with water molecules and thereby reduce plasma protein adherence on the hydrophilic surface.

29. The device of claim 28, wherein, when the catheter is inserted into the vein, the hydrophilic surface generates a layer of water on the hydrophilic surface, thereby creating a barrier to plasma protein adherence.

30. The device of claim 29, wherein the layer of water reduces the number of binding sites for blood platelet adhesion to the hydrophilic surface.

31. The device of claim 26, wherein the hydrophilic surface comprises a water contact angle of 20 degrees or less.

32. The device of claim 31, wherein the hydrophilic surface comprises a water contact angle of 10 degrees or less.

33. The device of claim 25, wherein the modified surface chemistry comprises a super- hydrophilic surface.

34. The device of claim 25, wherein the modified surface chemistry follows contours and roughness of the cage or the impeller.

35. The device of claim 29, wherein the layer of water comprises a thickness that is substantially equal to or greater than an average roughness (Ra) of a surface of the cage or the impeller.

36. The device of claim 25, wherein the cage and/or impeller comprises a metal and the modified surface chemistry of the cage and/or the impeller comprises a modification to an oxide layer of the metal.

37. The device of claim 36, wherein the metal comprises a transition metal from period 4, D- block of the periodic table and the oxide layer comprises an oxide of said period 4 transition metals.

38. The device of claim 25, wherein the cage and or the impeller comprises one of scandium, titanium, vanadium, chromium, manganese, iron, cobalt, nickel, copper, or zinc.

39. The device of claim 25, wherein the cage and/or impeller comprise a surface layer and the surface layer comprises an enriched concentration of titanium or chromium.

40. The device of claim 39, wherein the surface layer comprises a metal oxide of titanium or chromium said oxide further comprising titanium oxide (TiO), titanium dioxide (Ti02), dititanium trioxide (TΪ203), chromium (II) oxide (CrO), chromium (III) oxide (Cr203), chromium dioxide (Cr02), chromium trioxide (Cr03), chromium (IV) or a combination of these.

41. The device of claim 26, wherein the modified surface chemistry comprises attaching a hydrophilic functional group to the surface of the cage and/or impeller.

42. The device of claim 41, wherein the hydrophilic functional group comprises one or more of a hydroxy group, a carboxyl group, an amine group, a carbonyl group, a chloro group, an ether group, a phosphate group, or a sulphate group.

43. The device of claim 25, wherein the modified surface chemistry comprises a coating.

44. The device of claim 43, wherein the coating comprises a coating thickness and the coating thickness is greater than the average roughness (Ra) of the surface of the cage and impeller.

45. The device of claim 43, wherein the coating comprises at least one of a polysaccharide, a polymer, or a hydrogel.

46. The device of claim 43, wherein the coating comprises a polyurethane, polyethylene glycol, poly-2-oxazolines, polyvinyl alcohol, polyvinylpyrrolidone, maleic anhydride copolymer, poly(lactide-co-glycolide), aminoalkyl(meth)acrylamide, aminopropylmethacrylamide, poly- phosphorylcholine, polyethylene oxide, polyethylene succinate, polyethylene adipate, polyvinyl alcohol-co-ethylene, polyacrylic acid, copolymers and blends of the aforementioned.

47. The device of claim 45, wherein the polysaccharide comprises heparin.

48. The device of claim 25, wherein the modified surface chemistry comprises an altered oxide layer.

49. The device of claim 48, wherein the oxide layer is formed by electropolishing, heat treatment, or acid passivation.

50. The device of claim 25, wherein the modified surface chemistry exhibits hydrophilic properties such that the surface binds to water molecules to the exclusion of plasma proteins.

51. The device of claim 25, wherein the modified surface chemistry provides an increased surface wettability.

52. The device of claim 51, wherein the surface wettability has a contact angle measurement of less than 20 degrees.

53. The device of claim 25, wherein the cage comprises the modified surface chemistry.

54. The device of claim 25, wherein substantially all of the cage and/or the impeller that is exposed to blood when the catheter is operating inside the vein comprises the modified surface chemistry.

55. The device of claim 25, wherein the catheter further comprises a cuff, the cuff providing a smooth transition between an outer surface of the catheter and a proximal portion of the cage.

56. The device of claim 55, wherein the cuff comprises the modified surface chemistry.

57. The device of claim 25, wherein a distal portion of a shaft of the impeller and a distal portion of the cage defines a gap.

58. The device of claim 57, wherein at least one of the distal portion of the shaft or the distal portion of the cage defining the gap comprises the modified surface chemistry.

59. The device of claim 45, wherein the coating further comprises one of polyethyleneimine, polyurethane, a sulfonate group, albumin, a polyamine, polyvinyl siloxane, hyaluronic acid, or any combination thereof.

60. The device of claim 25, wherein the device further includes an expandable member attached to an exterior surface of the cage.

61. The device of claim 60, wherein the expandable member is a balloon.

62. The device of claim 61, wherein operating the catheter causes an increase in blood flow inside the vein.

63. The device of claim 62, wherein the device is for treating edema.

64. The device of claim 25, wherein the modified surface chemistry comprises a modification to an oxide layer and the thickness of said modification is less than 5,000 picometers.

65. The device of claim 64, wherein the modified surface chemistry comprises a layer thickness that is less than 3000 picometers.

66. The device of claim 65, wherein the modified surface chemistry comprises a layer thickness that is less than 2000 picometers.

67. The device of claim 66, wherein the modified surface chemistry comprises a layer thickness that is less than 1000 picometers.

68. The device of claim 25, wherein the modified surface chemistry comprises a first atom and a second atom, the first atom forming a chemical bond with an oxide layer and said second atom forming a bond with said first atom.

69. The device of claim 68, wherein the first atom comprising a first electronegativity and the second atom comprising a second electronegativity and the difference between said electronegativities is equal to or greater than 0 8

70. The device of claim 69, wherein the difference between the first electronegativity and said second electronegativity is equal to or greater than 1.0.

71. The device of claim 70, wherein the difference between the first electronegativity and said second electronegativity is equal to or greater than 1.2.

72. The device of claim 71, wherein the difference between the first electronegativity and said second electronegativity is equal to or greater than 1.5.

73. A device for treating edema, the device comprising: a catheter dimensioned for insertion into a vein, the catheter comprising a proximal portion and a distal portion; a cage attached to the distal portion of the catheter; and an expandable member attached to an exterior surface of the cage, wherein a portion of a surface of the expandable member is non-thrombogenic.

74. The device of claim 73, wherein the non-thrombogenic surface comprises a block copolymer comprising a first polymeric block and a second polymeric block.

75. The device of claim 74, wherein the first polymeric block comprises a hydrophilic functional group.

76. The device of claim 75, wherein, the second polymeric block comprises a polymer repeat unit selected to enhance flexibility in the second polymeric block.

77. The device of claim 76, wherein, the first and the second polymeric blocks are substantially immiscible and, when copolymerized, form phase separated blocks within a polymer matrix.

78. The device of claim 77, wherein the phase separation is manifested on the surface of the expandable member.

79. The device of claim 78, wherein the polymer comprises non-bound chemical species, the non-bound chemical species comprising oligomers and additives.

80. The device of claim 79, wherein the polymer is treated so as to remove the non-bound chemical species and further manifest the phase separation on the surface of the expandable member.

81. The device of claim 73, wherein the non-thrombogenic surface comprises a hydrophilic coating or a hydrophilic material.

82. The device of claim 81, wherein the hydrophilic coating or hydrophilic material binds to water molecules to the exclusion of blood plasma proteins, thereby preventing blood clots.

83. The device of claim 82, wherein the surface of the expandable member includes portions with the hydrophilic coating and portions without the hydrophilic coating.

84. The device of claim 83, wherein the one or more portions with the hydrophilic coating are configured for continuous contact with blood when the expandable member is in an expanded state.

85. The device of claim 84, wherein the one or more portions without the hydrophilic coating are configured to maintain a static contact with the vessel wall when the expandable member is in an expanded state.

86. The device of claim 73, wherein the expandable member comprises an expanded state, and in the expanded state, the expandable member is configured to maintain static contact with a wall of the vein, and wherein a pressure gradient across the expandable member is between ImmHg and 30 mmHg in the expanded state.

87. The device of claim 81, wherein the hydrophilic coating comprises one selected from the group consisting of a polysaccharide, a polymer, and a hydrogel.

88. The device of claim 87, wherein the polymer comprises a polymer with a hydrophilic chain segment.

89. The device of claim 88, wherein the polymer comprises a block copolymer with a hydrophilic block and a hydrophobic block, the hydrophobic block configured to bind to the surface of the expandable membrane.

90. The device of claim 87, wherein the polysaccharide comprises a polymeric derivative of heparin.

91. The device of claim 81, wherein the hydrophilic coating comprises more than half of the surface of the expandable member that is exposed to blood when the expandable member is in an expanded state inside the vein.

92. The device of claim 81, wherein the hydrophilic material comprises one of an aromatic polyurethane, an aliphatic polyurethane, a polyurethane comprising a copolymer of polytetramethylene glycol, a polyurethane comprising a copolymer of polyethylene glycol, a polyurethane comprising a copolymer of polypropylene glycol, a polyurethane comprising a copolymer of a polycarbonate glycol or a blend, copolymer or mixture of the above.

93. The device of claim 81 , wherein the expandable member is a balloon.

94. The device of claim 93, wherein upon expansion of the balloon, the balloon opposes a wall of a blood vessel and directs blood flow into an inlet of the cage.

95. The device of claim 93, wherein the cage comprises one or more outlets such that when the catheter is operating inside the vein blood moves through the cage and out of the one or more outlets.

96. The device of claim 95, wherein, when the catheter is operating inside the vein, flow dynamics of blood moving through the cage creates a low-pressure region adjacent a lymph duct, thereby urging fluid to drain from the lymph duct.

97. The device of claim 96, wherein the device is used for treating edema.

98. The device of claim 95, wherein upon expansion of the balloon, a distal-most portion of the balloon is aligned over the outlets to mitigate blood recirculation.

99. The device of claim 93, wherein the balloon comprises a collapsed state for delivery and an expanded state for treatment wherein, in the collapsed state, a membrane of the expandable member is substantially unstressed and in the expanded state the membrane is stressed by a balloon inflation pressure.

100. The device of claim 99, wherein transitioning to the expanded state comprises an unfolding of the membrane.

101. The device of claim 100, wherein the balloon comprises a tubular segment and the expanded state comprises a radial expansion of the balloon tubular segment.

102. The device of claim 101, wherein the radial expansion of the tubular segment comprises an increase in the circumference of the balloon of 300% or greater.

103. The device of claim 102, wherein the radial expansion of the tubular segment comprises an increase in the circumference of the balloon of 400% or greater.

104. The device of claim 103, wherein the radial expansion of the tubular segment comprises an increase in the circumference of the balloon of 500%.

105. The device of claim 101, wherein the radial expansion of the tubular segment comprises a biaxial elongation of a wall of the tubular segment.

106. The device of claim 105, wherein the radial expansion of the tubular segment comprises a circumferential elongation and an axial elongation of a balloon wall with both axial and circumferential elongations occurring approximately at the same time as the tubular segment expands.

107. The device of claim 99, wherein, in the expanded state, a surface of the expandable member that is exposed to blood while the catheter is operating inside the vein is non- thrombogenic.

108. The device of claim 93, wherein the balloon comprises an elastomer comprising one of thermoplastic polyurethane, polycarbonate urethane, aromatic polyurethane, thermoplastic rubber, aliphatic polyether-based urethane, thermoplastic silicone polycarbonate, or thermoplastic block copolymer.

109. The device of claim 101, wherein a balloon wall material comprises a resilient elastomer material with a low hysteresis loss ratio at human body temperature.

110. The device of claim 109, wherein the hysteresis loss ratio of the balloon wall material is less than 30% at a maximum test elongation of 300% at human body temperature.

111. The device of claim 110, wherein the hysteresis loss ratio of the balloon wall material is less than 20% at a maximum test elongation of 300% at human body temperature.

112. The device of claim 111, wherein the hysteresis loss ratio of the balloon wall material is less than 15% at a maximum test elongation of 300% at human body temperature.

113. The device of claim 109, wherein the balloon wall material comprises a low hysteresis loss ratio at human body temperature across a range of maximum test elongations and across a range of test times.

114. The device of claim 109, wherein the balloon wall material is configured to resist creep when inflated to a diameter of an innominate vein or superior vena cava vein.

115. The device of claim 114, wherein the balloon wall material creep resistance comprises returning the balloon to substantially its original deflated state after being inflated in to the diameter of the innominate vein or the superior vena cava vein and then re-inflating the balloon.

116. The device of claim 114, wherein the balloon wall material creep resistance comprises the external surface area of the deflated balloon remaining substantially unchanged after an inflation and deflation cycle to the diameter of the innominate vein or the superior vena cava vein at human body temperature.

117. The device of claim 116, wherein the inflation and deflation cycle comprises a plurality of inflation and deflation cycles over a time period of 24 hours.

118. The device of claim 117, wherein the inflation and deflation cycle comprises a plurality of inflation and deflation cycles over a time period of 72 hours.

119. The device of claim 73, wherein an exterior surface of the cage comprises a proximal attachment surface and a distal attachment surface with the expandable member attached to said proximal and distal attachment surfaces.

120. The device of claim 119, wherein said proximal and distal attachment surfaces comprise interstitial surfaces.

121. The device of claim 120, wherein the interstitial surfaces comprise a multiplicity of asperities and a plurality of interstices.

122. The device of claim 121, wherein attachment of the expandable member to the interstitial surfaces comprises an interpenetration of some of a material of the expandable member around the asperities of the interstitial surface and into the interstices of the interstitial surfaces.

123. The device of claim 120, wherein the interstitial surfaces comprise a surface roughness (Ra) that is equal to or greater than 1 micrometer.

124. The device of claim 123, wherein the interstitial surfaces comprise a surface roughness (Ra) that is equal to or greater than 3 micrometers.

125. The device of claim 124, wherein the interstitial surfaces comprise a surface roughness (Ra) that is equal to or greater than 9 micrometers.

126. The device of claim 119, wherein said proximal attachment surface and said distal attachment surface comprise a single tubular surface with a proximal end and a distal end.

127. The device of claim 101, wherein, in the expanded state, a wall thickness of the balloon is less than 50% of the wall thickness of the balloon in the collapsed state.

128. The device of claim 127, wherein, in the expanded state, the wall thickness of the balloon is less than 30% of the wall thickness of the balloon in the collapsed state.

129. The device of claim 127, wherein, in the expanded state, the wall thickness of the balloon is less than 20% of the wall thickness of the balloon in the collapsed state.

130. An intravascular device, the device comprising: a catheter dimensioned for inserting into a vein, the catheter comprising a proximal portion and a distal portion; and a cage attached to the distal portion of the catheter, the cage housing an impeller, wherein a portion of a surface of the cage or the impeller comprises a non-thrombogenic metallic interface.

131. The device of claim 130, wherein the non-thrombogenic metallic interface comprises a primary metallic element that is selected from period 4 transition metals of the periodic table of elements.

132. The device of claim 131, wherein the period 4 transition metal comprises one of titanium, vanadium, chromium, iron, cobalt, or nickel.

133. The device of claim 132, wherein the non-thrombogenic metallic interface further comprises a secondary metallic element that comprises one of:

(i) an element from the group of period 4 transition metals;

(ii) molybdenum; or

(iii) tungsten, gold, tantalum or platinum.

134. The device of claim 133, wherein the non-thrombogenic metallic interface comprises an alloy.

135. The device of claim 134, wherein the alloy comprises a chromium alloy or titanium alloy.

136. The device of claim 135, wherein the chromium alloy comprises a stainless-steel alloy or a cobalt chromium alloy.

137. The device of claim 135, wherein the titanium alloy comprises a nitinol, Ti6A14V or 4TITUDE.

138. The device of claim 137, wherein the nitinol comprises a low level of inclusions or impurities.

139. The device of claim 136, wherein the cobalt chromium alloy is a non-magnetic alloy.

140. The device of claim 131, wherein the metal comprises a metal grade associated with a low level of undesirable impurities comprising nitride, sulfide, silicate, phosphide, carbide, or hydride impurities.

141. The device of claim 130, wherein the non-thrombogenic metallic interface comprises an oxygen active material.

142. The device of claim 141, wherein the non-thrombogenic metallic interface comprises an oxide of said oxygen active material.

143. The device of claim 142, wherein the oxygen active material comprises titanium or chromium or aluminum.

144. The device of claim 130, wherein a surface of the non-thrombogenic metallic interface comprises an oxide film.

145. The device of claim 144, wherein the cage or the impeller comprises a metallic substructure that is enveloped with a continuous oxide film that defines an exterior surface of the cage or the impeller.

146. The device of claim 145, wherein the oxide film comprises an oxide film of a metallic element of said metallic substructure.

147. The device of claim 146, wherein the oxide film is configured so as to substantially preclude oxides of thrombogenic metallic elements or promote oxides of non-thrombogenic elements.

148. The device of claim 147, wherein the oxide film is configured to promote titanium dioxide or chromium oxide.

149. The device of claim 147, wherein the oxide film is configured to preclude oxides of nickel, iron, cobalt, copper and zinc.

150. The device of claim 147, wherein the oxide film comprises Ti02 or Cr203 or A1203 or a mixture of two or more of these oxides.

151. The device of claim 147, wherein at least 90% of the metal content of the oxide film comprises Ti02 or Cr203 or A1203 or a mixture thereof.

152. The device of claim 151, wherein at least 95% of the metal content of the oxide film comprises Ti02 or Cr203 or A1203 or a mixture thereof.

153. The device of claim 152, wherein at least 98% of the metal content of the oxide film comprises Ti02 or Cr203 or A1203 or a mixture thereof.

154. The device of claim 152, wherein the non-thrombogenic metallic interface comprises a plurality of hydrophilic groups attached to the oxide film.

155. The device of claim 152, wherein the attachment of a plurality of hydrophilic groups comprises a chemical attachment of said reactive groups to the oxide film.

156. The device of claim 130, wherein the cage has the non-thrombogenic metallic interface.

157. The device of claim 156, wherein substantially all of the surface of the cage or the impeller that is in contact with blood when the catheter is inside the vein comprises the non- thrombogenic metallic interface.

158. The device of claim 130, wherein the non-thrombogenic metallic interface comprises a transition metal or a post-transition metal.

159. The device of claim 158, wherein the non-thrombogenic metallic interface comprises one of titanium, cobalt, nickel, zirconium, gold, silver, or iridium, aluminum, tantalum, stainless steel, or nickel titanium.

160. The device of claim 130, wherein the non-thrombogenic metallic interface exhibits hydrophilic properties that inhibit blood clots while the catheter is inside the vein.

161. The device of claim 130, wherein the catheter further includes a cuff attached to a proximal portion of the cage.

162. The device of claim 161, wherein the cuff comprises the non-thrombogenic metallic interface.

163. The device of claim 162, wherein substantially all of the cuff that is in contact with blood when the catheter is inside the vein comprises the non-thrombogenic metallic interface.

164. The device of claim 130, wherein the vein is a jugular vein.

165. The device of claim 130, wherein the catheter further includes an expandable member attached to an exterior surface of the cage.

166. The device of claim 165, wherein the expandable member is a balloon.

167. The device of claim 165, wherein, when the distal portion of the catheter is inside the vein, the expandable member is inflated and the impeller is activated so as to draw blood through the cage.

168. The device of claim 167, wherein a flow of blood through the cage reduces pressure near a lymph duct.

169. The device of claim 168, wherein the device is useful for treating edema.

170. The device of claim 130, wherein a cross-sectional diameter of an outer wall of the cage is greater at a proximal portion than at a distal portion of the cage.

171. The device of claim 130, wherein the catheter further comprises an atraumatic tip extending from a distal portion of the cage.

172. The device of claim 171, wherein the atraumatic tip comprises polyether ether ketone.

173. The device of claim 130, wherein a diameter of the catheter is from about 6 Fr to about

12 Fr.

174. The device of claim 154, wherein the plurality of hydrophilic groups attached to the oxide film comprises a triol.